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# Registrar Corp: At Registrar Corp, compliance made quick and easy™ is our goal. We work tirelessly to help bring our clients’ products to market — wherever they are in the world. With our team of dedicated regulatory professionals, we make sure they never have to handle compliance alone.
## Pages
- [File Notifications (CPNP, SCNP)](https://www.registrarcorp.com/cosmetic-notification-cpnp-scnp/): We prepare, validate, and file your CPNP and SCPN notifications end-to-end so your cosmetics reach EU and UK shelves faster, your records hold up at inspection, and your team never deciphers another portal.
- [Southeast Asia – Maritime Office](https://www.registrarcorp.com/contact/southeast-asia-maritime/): Registrar Corp has been the leader across Southeast Asia’s island nations for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [India Hyderabad Office](https://www.registrarcorp.com/contact/india-hyderabad-office/): Registrar Corp has been the leader in India for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [Africa – Sub-Saharan Office](https://www.registrarcorp.com/contact/africa-sub-saharan-office/): Registrar Corp has been the leader in Africa for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [China Office](https://www.registrarcorp.com/contact/china-office/): Registrar Corp has been the leader in China for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [United Kingdom Ireland](https://www.registrarcorp.com/contact/united-kingdom-ireland/): Registrar Corp has been the leader in the UK and Ireland for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [Korea Office](https://www.registrarcorp.com/contact/korea-office/): Registrar Corp has been the leader in Korea for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [South America Office](https://www.registrarcorp.com/contact/south-america-office/): Registrar Corp has been the leader in South America for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help, we look forward to partnering in the growth of your business.
- [European Union](https://www.registrarcorp.com/contact/european-union/): Registrar Corp has been the European leader for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help, we look forward to partnering in the growth of your business.
- [Central America Office](https://www.registrarcorp.com/contact/central-america-office/): Registrar Corp has been the leader in Central America for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help, we look forward to partnering in the growth of your business.
- [India Kurnool Office](https://www.registrarcorp.com/contact/india-kurnool-office/): Registrar Corp has been the leader in India for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [Mexico Office](https://www.registrarcorp.com/contact/mexico-office/): Registrar Corp has been the leader in Mexico for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [South Asia Mainland Office](https://www.registrarcorp.com/contact/southeast-asia-mainland/): Registrar Corp has been the leader in Southeast Asia for U.S. regulatory compliance and global market access for over 20 years. Please let us know how we can help. We look forward to partnering in the growth of your business.
- [LACF & Acidified (FCE/SID) Compliance](https://www.registrarcorp.com/low-acid-canned-foods-acidified-foods-compliance/): Registrar Corp and TechniCAL combine FDA regulatory expertise with Process Authority science to deliver complete compliance for low-acid canned foods (LACF) and acidified foods.
- [Global Representation](https://www.registrarcorp.com/medical-devices/global-representation/): For medical devices and in vitro diagnostic devices (IVDs), many regulatory frameworks worldwide require manufacturers that are not established in the country where they intend to sell their products to appoint a local in-country representative. We act as your representative and your primary point of contact with local authorities to ensure smooth communications and continuous regulatory compliance.
- [Free Sale Certificates](https://www.registrarcorp.com/medical-devices/fsc-free-sale-certificates/): Registrar Corp helps medical device manufacturers secure Free Sale Certificates efficiently, accurately, and with confidence — as part of a complete global regulatory compliance strategy.
- [Global Registration](https://www.registrarcorp.com/medical-devices/global-registration/): Registrar Corp’s global network of trusted compliance experts will ensure that your medical devices can go to market efficiently and safely. Simplify and strengthen your business with a single compliance partner for every medical device, in every market.
- [Protect your company against gray marketing and distribution violations](https://www.registrarcorp.com/guardian/): Guardian™ by Registrar Corp protects your company against gray marketing and distribution violations.
- [Food manufacturing training topics and eLearning library](https://www.registrarcorp.com/workforce-training/elearning-library/): There’s a direct line between the quality of your training program and your bottom line. Better training leads to more engaged and capable employees, which leads to quality and production improvements and fewer injuries. Harness the power of a world-class training library to drive better outcomes in your facility.
- [LMS Learning Management System for Food Manufacturing](https://www.registrarcorp.com/workforce-training/lms-learning-management-system/): Streamline onboarding, automate audit preparation, and strengthen engagement with workforce development features. SkillUp™ frontline worker training platform provides a full-feature, user-friendly learning management system (LMS) to simplify your workforce training.
- [AI Course Creation, Course Authoring & SOP Training Software](https://www.registrarcorp.com/workforce-training/course-creation-software/): Create custom training courses in minutes, not days, with SkillUp’s AI Create feature. Whether you’re AI-savvy or a first-time AI user, you’ll be able to create custom eLearning training courses in minutes with this easy but powerful course authoring software.
- [MoCRA Compliance](https://www.registrarcorp.com/services/mocra-compliance/): From small, independent brands to well-established cosmetic giants, we simplify FDA MoCRA compliance so cosmetic companies of any size can distribute cosmetic & personal care products confidently & safely.All cosmetic facilities must register with FDA. We can register your facility and serve as US Agent for Non-US facilities.FDA requires all products to be listed. We help you save time, money, and the frustration of doing it yourself.Adverse Events must be collected, investigated, and reported to FDA. 
Our Adverse Events Management software assures compliance.MoCRA changes product labeling requirements. Our experienced specialists assure your cosmetic labels meet new FDA standards.Accelerate product development and compliance with Cosmetri, our GMP and cosmetic formulation software.Professionally train your QA/QC and compliance staff on GMP, MoCRA, ISO 22716, and GLP with our expert online training courses.Whether you want full-service support or early expert validation, we help you meet the state’s additional cosmetic requirements.Full-service California compliance.We review your complete formula, perform ingredient and cumulative concentration analysis, and help you identify if a Prop 65 warning is needed on your label. Ideal for brands that want total compliance confidence and a hands-off path to California readiness.Early insight for teams that stay hands-on.We provide ingredient-level review and visibility into California considerations so your R&D or regulatory team can make informed decisions early. Reporting support can be made available when you need it.
- [Referral](https://www.registrarcorp.com/referral/): Registrar Corp has been a global leader since 2003 for regulatory compliance and workforce training. More than 30,000 clients in over 150 countries trust and rely on Registrar’s expertise, with our commitment to unsurpassed service for every single client.
- [Cosmetri – Manufacturers](https://www.registrarcorp.com/software/cosmetri/manufacturers/): Run production with digital discipline: batch records, CAPA, EDMS, complaints/recalls, SUE/OOS, KPIs — aligned to ISO 22716.
- [Cosmetri Brand](https://www.registrarcorp.com/software/cosmetri/brands/): Connect marketing briefs to compliant formulations, packaging, and cost — so every launch hits timelines and margins.
- [Cosmetri – R&D Quality](https://www.registrarcorp.com/software/cosmetri/rd-quality/): Keep formulas, documentation, and quality data in sync — from the formulation labs to market release.
- [Cosmetri – Persona Hub](https://www.registrarcorp.com/software/cosmetri/): Cosmetri Product Manager (PLM) — formulation, compliance checks, testing, packaging & cost, clean handoff to production. (Includes 40K+ safe ingredients/chemicals selector.)
- [Simplify FDA Compliance for Exporters to US](https://www.registrarcorp.com/services/food-safety/fda-compliance-for-food-exports/): Gain full FDA compliance to export food to the U.S. with one trusted partner. No gaps. No delays. Just confidence.
- [SkillUp Workforce Training Solution](https://www.registrarcorp.com/workforce-training/): Level up your workforce training program with SkillUp™ — a modern, flexible platform built for today’s food manufacturing industry. SkillUp’s comprehensive library of eLearning courses, user-friendly learning management system (LMS), and AI course creator offer flexible food manufacturing training solutions that can be tailored to your needs.
- [Workforce Training Savings Assessment Calculator](https://www.registrarcorp.com/workforce-training/savings-assessment-tool/): You could save up to $0 by using SkillUp for your workforce training.
- [US Agent](https://www.registrarcorp.com/industries/medical-devices/services/us-agent-for-medical-devices/): Medical device companies, based outside the US must appoint a US Agent to register with FDA. Without one, your shipments risk delays, detentions, or refusal.
- [Unique Device Identifier (UDI/GUDID)](https://www.registrarcorp.com/industries/medical-devices/services/udi-gudid-compliance/): Creating and submitting Unique Device Identifiers (UDIs) can be time-consuming and complex. Registrar Corp simplifies the process by helping medical device labelers comply with FDA UDI regulations and submit their data to the Global Unique Device Identification Database (GUDID).
- [Master Files](https://www.registrarcorp.com/industries/medical-devices/services/master-files/): Master Files are secure regulatory documents used to protect proprietary product data while supporting approval applications for medical devices, drugs, biologics, and veterinary products.
- [Import Alerts](https://www.registrarcorp.com/industries/medical-devices/services/medical-device-import-alerts/): Import Alerts can halt shipments and trigger costly delays. If listed, your products may face automatic detention (DWPE). To resume trade, you must prove compliance through corrective actions and repeated clean shipments. Registrar Corp guides you through the removal process with expert, FDA-ready petitions..
- [Export Certificate](https://www.registrarcorp.com/industries/medical-devices/services/us-fda-medical-device-export-certificate/): When exporting FDA-regulated products from the United States, foreign customers or governments often require an Export Certificate as proof that your product complies with US regulations. These certificates confirm a product’s regulatory or marketing status, helping to streamline customs clearance and facilitate international trade.
- [Health Canada – Cosmetics Compliance](https://www.registrarcorp.com/industries/cosmetics/health-canada-cosmetics-compliance/): We manage every requirement — CNFs, Hotlist reviews, bilingual labels, and Responsible Person services so your products meet Health Canada standards without delay.

## Events

## Case Studies
- [Cosmetri empowers CR Formulations to achieve GMP compliance and scale](https://www.registrarcorp.com/resources/case-studies/cosmetri-empowers-cr-formulations-to-achieve-gmp-compliance-and-scale/): Once CR Formulations chose Cosmetri®, the benefits were instant. The company was able to set up the user-friendly software and begin preparing for their GMP certification immediately.
- [Cosmetri helps Cosmetics Labs Australia scale for growth](https://www.registrarcorp.com/resources/case-studies/cosmetri-helps-cosmetics-labs-australia-scale-for-growth/): Cosmetics Labs Australia needed cost-effective software that would satisfy their management and compliance needs.
- [Happy Farm Botanicals Case Study](https://www.registrarcorp.com/resources/case-studies/happy-farm-botanicals-case-study/): How Happy Farm Botanicals Optimized Operations and Expanded Its Brand Portfolio with Cosmetri®
- [Cosmetri unlocks operational efficiency for Niche Skin Labs](https://www.registrarcorp.com/resources/case-studies/cosmetri-unlocks-operational-efficiency-for-niche-skin-labs/): Niche Skin Labs discovered a need for an end-to-end cosmetics formulation development software to improve efficiency and save time for product development.
- [Registrar Corp helps family business Italian Imports achieve FSVP compliance](https://www.registrarcorp.com/resources/case-studies/italian-imports-fsvp-compliance/): 2019 FSVP requirements force small family business Italian Imports to seek professional regulatory compliance support. 5 years later Registrar Corp is helping keep Italian Imports in business
- [Pong Chien passes FSVP inspections with Registrar Corp](https://www.registrarcorp.com/resources/case-studies/pong-chien-fsvp-inspections/): International importer Pong Chien needed help preparing for an FDA inspection and developing FSVPs. 5 years later, Registrar Corp is still their first choice for FSVP compliance.
- [Online Training enables PL Developments to scale safely](https://www.registrarcorp.com/resources/case-studies/online-training-enables-pl-developments-to-scale-safely/): PL Developments needed online PCQI and HAACP training for their team to take on larger contracts. Registrar Corp’s Online Training platform gave them the tools to expand.
- [Registrar Corp’s PCQI training helps Dyne Bio export new superfood to the U.S.](https://www.registrarcorp.com/resources/case-studies/pcqi-training-dyne-bio-superfood-us/): Korean bio-healthcare Dyne Bio has to become FSVP-compliant to bring their red algae product to the U.S.. Registrar Corp’s Online Training helps them become PCQI trained and expand their business.
- [Lipari Foods successfully monitors 40+ suppliers and saves $50k per shipment](https://www.registrarcorp.com/resources/case-studies/lipari-40-suppliers-50k-complyhub/): Wholesale food distributor Lipari struggled to monitor and source suppliers manually and needed an FSVP compliance solution. With Registrar Corp’s ComplyHub™, they were able to streamline and save.
- [How wholesaler Nathel & Nathel saved 500 hours a month](https://www.registrarcorp.com/resources/case-studies/how-wholesaler-nathel-nathel-saved-500-hours-a-month/): When Nathel & Nathel received a supplier FDA Import Alert, they faced potential penalty costs and business loss. Registrar Corp’s ComplyHub™ enabled them to automate FSVP monitoring and gain compliance.
- [How retail giant TJX monitors 1,000+ suppliers with ComplyHub™](https://www.registrarcorp.com/resources/case-studies/how-tjx-monitors-1000-suppliers-with-complyhub/): Multinational department store corporation TJX needed a better solution for monitoring 1,000+ suppliers. With Registrar Corp’s ComplyHub™, they were able to streamline FSVP compliance.
- [Registrar Corp saves wholesale importer over $50,000 annually](https://www.registrarcorp.com/resources/case-studies/registrar-corp-saves-wholesale-importer-over-50000-annually/): A U.S. importer’s lack of FSVP documentation exposed them to fees and reputation loss. With Registrar Corp’s regulatory expertise and ComplyHub solution, they gained compliance and saved over $50k.
- [ComplyHub™ identifies 20x more suppliers for U.S. importer](https://www.registrarcorp.com/resources/case-studies/complyhub-identifies-20x-more-suppliers/): This U.S. food importer received an FDA Warning Letter for misidentifying suppliers. Our expert guidance and ComplyHub solution helped them uncover 90+ suppliers and save thousands in costs and FDA fees.
- [Small business saves $16,000+ annually with FSVP compliance with ComplyHub™](https://www.registrarcorp.com/resources/case-studies/small-business-saves-16000-annually-with-complyhub/): A small U.S. importer with no FSVP plan or documents received an FDA Warning Letter. With Registrar Corp’s guidance and Automated Compliance Marketplace, they were able to gain compliance.
- [How ComplyHub™ helped wholesale importer save over $60,000 annually](https://www.registrarcorp.com/resources/case-studies/complyhub-saves-wholesale-importer-over-60000-annually/): This U.S. importer was not properly monitoring suppliers which exposed them to FDA penalties. Registrar Corp’s ComplyHub solution helped them streamline compliance and save over $60k.

## Free Tools

## Blogs
- [European Regulatory Agencies and Market Access: Understanding HMA, EDQM, Swissmedic, and MHRA ](https://www.registrarcorp.com/blog/drugs/understand-hma-edqm-swissmedic-mhra/): While the European Medicines Agency (EMA) remains central to many pharmaceutical approvals, Europe’s regulatory framework extends well beyond a single authority. Organizations such as the Heads of Medicines Agencies (HMA), the European Directorate for the Quality of Medicines & HealthCare (EDQM), Swissmedic, and the Medicines and Healthcare products Regulatory Agency (MHRA) each play important roles in shaping how medicines are reviewed, monitored, and maintained throughout their lifecycle. Together, these organizations illustrate how European regulation has evolved from independent national systems into a coordinated ecosystem balancing regulatory oversight, quality standards, and market access. 
- [FDA Expands Sunscreen Options for the First Time in 20 Years: What Bemotrizinol Addition Means for Manufacturers ](https://www.registrarcorp.com/blog/drugs/drug-regulations/fda-sunscreen-approval-bemotrizinol/): The U.S. Food and Drug Administration (FDA) has taken a significant step toward modernizing sunscreen regulation by adding bemotrizinol as a permitted active ingredient in over-the-counter (OTC) sunscreen products. This marks the first time in more than two decades that the FDA has expanded the list of approved sunscreen active ingredients. 
- [EU Fragrance Allergen Labeling Requirements: What Cosmetic Brands Need to Know Before July 2026](https://www.registrarcorp.com/blog/cosmetics/eu-fragrance-allergen-regulation-labeling-requirements/): For decades, fragrance has occupied a unique position in the beauty industry. 
- [2026 FDA Food Facility Registration Renewal: What Food Exporters Need to Know ](https://www.registrarcorp.com/blog/food-beverage/fda-renewal-2026-ffr-registration/): The U.S. Food and Drug Administration (FDA) requires most registered food facilities to renew their FDA Food Facility Registration every even-numbered year. The next biennial renewal period will take place from October 1 through December 31, 2026. Thus, the time is now to prepare for FDA Renewal 2026.
- [Australia Drug Master Files: Regulatory Expectations and Business Impact](https://www.registrarcorp.com/blog/drugs/drug-master-files/australia-drug-master-files-regulatory-expectations/): Australia’s pharmaceutical regulatory environment places strong emphasis on manufacturing transparency, product quality, and accurate technical documentation. 
- [Already Exporting to the U.S.? Here’s Why You May Still Be Out of FDA Compliance](https://www.registrarcorp.com/blog/food-beverage/fsma/exporting-to-us-out-of-fda-compliance/): If your goal is to export confidently, without relying on luck or past performance, begin with FDA Compliance for Food Exports | Complete Compliance.
- [How Pharmaceutical Companies Can Simplify Active Substance Master File Procedures](https://www.registrarcorp.com/blog/drugs/active-substance-master-file-procedure/): Over the years, Active Substance Master File (ASMF) management has become increasingly complex for pharmaceutical companies supplying APIs to the European market. Regulatory expectations continue to evolve, electronic submission standards require greater precision, and even minor administrative errors can delay approvals or disrupt product timelines. 
- [FSVP Continuity Insurance: Protecting Your U.S. Market Access from Regulatory Friction](https://www.registrarcorp.com/blog/food-beverage/fsvp-documentation-protect-us-market-access/): In the high-stakes environment of international food trade, market access is far more than a regulatory hurdle; it is a hard-earned commercial asset. For established exporters, the primary strategic goal naturally shifts from the initial effort of entry to the critical preservation of continuity. Years of investment in distribution networks, relationship-building with retailers, and brand-positioning can be jeopardized by a single administrative lapse at the border.
- [How Much Does Safety Training Really Cost a Business — And What Happens If You Skip It?](https://www.registrarcorp.com/blog/food-beverage/true-cost-safety-training/): Most businesses think they know the cost of safety training: a per‑seat price, a few hours off the floor, and a line item that competes with production needs. But the real cost of safety training isn’t the invoice, it’s the gap between what a workforce understands and what the work environment demands of them. When that gap widens, expenses rise silently, long before an incident or citation ever occurs.
- [Why FDA Is Detaining More API & Bulk Ingredient Shipments — and How to Avoid It](https://www.registrarcorp.com/blog/drugs/fda-detaining-more-api-bulk-ingredient-shipments/): FDA enforcement is changing—and API (active pharmaceutical ingredient) and bulk ingredient manufacturers are feeling the impact at the border. Shipments that once cleared without issue are now being detained for compliance gaps that are entirely preventable. In many cases, the problem is not complex regulatory failure—it’s missing or incorrect information in FDA registrations and listings. 
- [The PFAS Threshold Trap: Why “Intentional Use” is No Longer the Standard for Cosmetics Compliance](https://www.registrarcorp.com/blog/cosmetics/cosmetics-pfas-threshold-trap/): For years, many global cosmetics brands have operated under a comfortable regulatory assumption: if they do not intentionally add ’forever chemicals’ (PFAS) to their formulations, they are insulated from the growing wave of PFAS restrictions. This ’intentional use’ standard allowed brands to rely on simple qualitative checks and marketing-led ingredient exclusions.
- [What is OMUFA? A Complete Guide to FDA Fees and Compliance for OTC Drug Manufacturers](https://www.registrarcorp.com/blog/drugs/drug-regulations/what-is-omufa/): For decades, the regulation of over-the-counter (OTC) drugs in the United States remained largely unchanged, relying on a slow, cumbersome rulemaking process. That shifted fundamentally with the passage of the Coronavirus Aid, Relief, and Economic Security (CARES) Act in 2020, which authorized the Over-the-Counter Monograph Drug User Fee Program (OMUFA).
- [From Idea to Launch Without the Rework: A Stage-Gate Framework for 2026 Cosmetics Compliance](https://www.registrarcorp.com/blog/cosmetics/cosmetic-regulations/stage-gate-framework-for-2026-cosmetics-compliance/): Five regulatory deadlines land on cosmetic brands in 2026 — most within the same six-month window. MoCRA biennial renewal opens across the US. Canada’s SOR/2024-63 fragrance-allergen rules take effect in two phases. The EU’s Omnibus VIII CMR restrictions activate with no sell-through runway. EU Regulation 2023/1545 expands fragrance-allergen labeling. State PFAS bans continue rolling across the US. 
- [What U.S. Importers Actually Expect from Foreign Suppliers Under FSVP](https://www.registrarcorp.com/blog/food-beverage/food-safety/what-importers-expect-under-fsvp/): In the world of international trade, there is a technical truth that many foreign suppliers use as a shield: the Foreign Supplier Verification Program (FSVP) is the legal responsibility of the U.S. importer. Technically, this is correct. It is the importer who must develop the program, conduct the verification, and face the FDA during an inspection to prove they have performed their due diligence.
- [How to Replace Your Current LMS Without Disrupting Operations](https://www.registrarcorp.com/blog/food-beverage/food-safety/how-to-replace-your-current-lms/): For HR and operations leaders, the decision to switch a learning management system (LMS) is rarely about whether the current system is ’good enough.’ Most know exactly when their platform has become a bottleneck.
- [The Defensible Blueprint: Strengthening Workforce Competency for the Modern FDA Inspection](https://www.registrarcorp.com/blog/food-beverage/food-safety/fda-inspection-training-defense/): When an FDA inspection investigator walks through your doors, they are evaluating the integrity of your entire facility. While workforce training is only one component of a comprehensive inspection, it often serves as the ’litmus test’ for your broader safety culture. They aren’t just looking for your training logs; they are looking for the ’why’ and the ’how’ behind your staff’s competency to determine if your operational guardrails are actually holding.
- [Workforce Training Software for Food Manufacturing: What Actually Reduces Audit Risk?](https://www.registrarcorp.com/blog/food-beverage/food-safety/workforce-safety-training-reduces-audit-risk/): When evaluating workforce safety training software, many facilities make the mistake of looking for HR infrastructure—a place to house documents and track basic onboarding. But in a high-stakes regulatory environment, your training software shouldn’t just be an administrative tool. It should be your audit armor.
- [From Fragmentation to Command: How to Monitor, Manage, and Control Foreign Suppliers](https://www.registrarcorp.com/blog/food-beverage/food-safety/foreign-supplier-management/): For most compliance teams, foreign supplier management feels like a game of defensive catch-up.
- [FSVP Procedures: Supplier Approval, Verification, and Re-Evaluation](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-procedures-overview/): This article provides sample FSVP procedures that importers can use as templates or benchmarks. Each example highlights what FDA expects to see in writing, what records should support the procedure, and where companies most often fall short.
- [The Global Exporter’s Blueprint: Navigating U.S. Market Growth with Unified FDA Compliance](https://www.registrarcorp.com/blog/food-beverage/food-facility-registration/unified-fda-compliance/): For food manufacturers across the globe, the U.S. market is often the ’North Star’ of global expansion—a high-volume, high-value destination that can transform a company’s trajectory. However, the wall protecting that market isn’t built of bricks, but of data, documentation, and a complex web of FDA compliance expectations.
- [How the SQF Edition 10 Food Safety Culture Requirements Will Transform Compliance](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-edition-10-food-safety-culture/): With the release of SQF Edition 10, the Safe Quality Food Institute (SQFI) has taken a significant step in strengthening food safety management systems by formally elevating food safety culture into a structured and auditable requirement.
- [FDA Registration Is Not Enough: Why True Export Compliance Requires Layered Requirements](https://www.registrarcorp.com/blog/food-beverage/food-facility-registration/fda-registration-is-not-enough/): Many foreign suppliers operate under a dangerous assumption: that FDA registration for their facility is the finish line for U.S. export compliance. While registration is a mandatory first step, it is merely one component of a much larger, high-stakes system.
- [Registrar’s SQF Training: Proven to Build Audit-Ready Confidence](https://www.registrarcorp.com/blog/food-beverage/food-safety/audit-ready-sqf-training/): When QA managers and food safety leaders evaluate an SQF training provider, they aren’t simply comparing course descriptions—they are assessing whether the provider can build real-world competence that holds up in front of an auditor. At the end of every certification cycle, what matters is whether your Practitioner can interpret complex clauses, defend critical decisions with objective evidence, maintain documentation discipline, lead rigorous internal audits, and guide the organization through the transition to Edition 10 with clarity and poise.
- [SQF Edition 10: The Transition Checklist for QA Managers](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-edition-10-checklist/): This checklist reinforces those fundamentals with practical, step-by-step preparation. It ensures teams have the structure, clarity, and confidence they need to transition smoothly into Edition 10—eliminating guesswork and the risks associated with waiting until the last minute.
- [Common SQF Non-Conformances and How to Prevent Them](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-non-conformances/): This article identifies where these systems most often collapse and why these gaps frequently escalate into major non-conformances during an audit cycle. By understanding the root causes of these common findings, facility leadership can move from reactive correction to proactive prevention.
- [How to Prepare for Your Next SQF Audit (Post-Edition 10)](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-audit-edition-10/): SQF audits do not reward last‑minute preparation. They reward systems that operate consistently, produce reliable records, and withstand scrutiny during both internal and external evaluations. With the transition to Edition 10, food safety managers and internal auditors are focusing on a unique challenge: how to build confidence in their systems when the updated Code emphasizes deeper behavioral and governance expectations.
- [SQF 10 vs. SQF 9: What Changed and Why It Matters](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-edition-10-vs-sqf-9/): SQF Edition 10 represents the next significant step in the effort to strengthen clarity and alignment with growing global food safety expectations. This update is designed to ensure that certified sites are not just complying with a set of rules, but are operating within a robust, proactive management system. This article highlights the essential changes you will see in Edition 10 and how they impact your facility’s path to certification.
- [What SQF Edition 10 Means for Food Manufacturers: A Strategic Evolution](https://www.registrarcorp.com/blog/food-beverage/food-safety/sqf-edition-10-readiness/): SQF certification remains one of the most widely recognized markers of operational integrity in the global food industry. With the release of Edition 10, manufacturers are preparing for a code that brings clearer expectations, stronger alignment with global standards, and a renewed emphasis on the behavioral side of compliance, specifically Food Safety Culture.
- [What Foreign Food Exporters Get Wrong About FDA Compliance (And Why It Costs Them)](https://www.registrarcorp.com/blog/food-beverage/food-safety/what-food-exporters-get-wrong/): Foreign food exporters don’t usually learn they misunderstood FDA compliance until a shipment is already detained, delayed, or refused at the border. By that point, the cost isn’t theoretical—it’s demurrage fees, spoiled product, missed contracts, and urgent calls to fix something that should have been addressed months earlier.
- [The Most Common Reasons FDA Stops Foreign Shipments at the Border (And Why They’re Entirely Preventable)](https://www.registrarcorp.com/blog/food-beverage/food-safety/reasons-for-fda-detentions/): Every week, FDA stops foreign food shipments that were otherwise destined for smooth entry into the United States with detentions and refusals. For many exporters, these holds feel unexpected—surprising even—but from FDA’s perspective, they are predictable outcomes of missing documentation, weak controls, or incomplete FSVP support.
- [FDA Will Not “Guide You Through” Export Compliance: What Foreign Suppliers Must Understand Before Shipping](https://www.registrarcorp.com/blog/food-beverage/food-safety/avoiding-fda-detentions/): Many foreign suppliers assume the U.S. Food and Drug Administration will offer direction, feedback, or pre-shipment guidance on what they must do to comply and avoid FDA detentions before exporting food to the United States. It’s an understandable assumption—many global regulators do provide this kind of support. FDA does not.
- [FSVP Procedures: Supplier Approval, Verification, and Re-Evaluation](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-procedures/): This article provides sample FSVP procedures that importers can use as templates or benchmarks. Each example highlights what FDA expects to see in writing, what records should support the procedure, and where companies most often fall short.
- [The True Cost of a Noncompliant Export: Why One FDA Action Can Undo Years of Market Access](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-fda-enforcement/): Foreign suppliers often assume FDA enforcement is temporary—a frustrating delay, an unexpected document request, or a single refusal that can be corrected quickly. But in practice, one FDA action can undo years of dependable market access. A single detention can trigger importer hesitation. A refusal can interrupt purchase cycles. An Import Alert can erase entire distribution networks. What feels like one isolated event to the supplier can permanently alter how U.S. buyers perceive your reliability.
- [How Medical Device Companies Can Overcome EUDAMED 2026 Registration Challenges](https://www.registrarcorp.com/blog/medical-devices/medical-device-registration/eudamed-2026-registration/): The European Union’s EUDAMED database is moving toward mandatory use under the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). While many manufacturers are aware of the system, fewer understand the operational work required to successfully register devices before the following upcoming regulatory deadlines:
- [Correcting an FSVP Violation: A Step-by-Step Plan to Restore Compliance Confidence](https://www.registrarcorp.com/blog/food-beverage/food-safety/correcting-an-fsvp-violation/): Receiving an FDA observation or Warning Letter for an FSVP violation can feel overwhelming. Most importers first experience it as a moment of uncertainty—a sharp realization that their records, supplier approvals, or verification activities were not as complete or defensible as they believed. But FSVP violations are correctable, and FDA’s process is more structured than many expect.
- [Importer of Record vs. FSVP Importer vs. U.S. Agent: Who Does What?](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-importer-ior-agent/): Many importers assume these three roles overlap—or worse, that they’re interchangeable. In reality, Importer of Record, FSVP Importer, and U.S. Agent are distinct regulatory identities governed by different authorities, responsibilities, and liabilities.
- [How FSVP Audits Actually Work (and Where Importers Get Caught)](https://www.registrarcorp.com/blog/food-beverage/food-safety/how-fsvp-audits-work/): Most importers feel confident in their Foreign Supplier Verification Program until one moment: the FDA issues a Notice of Inspection. What catches companies off guard isn’t the inspection itself—it’s the speed, precision, and record-centered depth with which investigators evaluate whether your FSVP exists, is implemented correctly, and actually reflects the risks in your supply chain.
- [How PCQI Training Supports—but Does Not Replace—FSVP](https://www.registrarcorp.com/blog/food-beverage/food-safety/pcqi-training-supports-fsvp/): Many importers assume that having a Preventive Controls Qualified Individual (PCQI) on staff automatically satisfies the Foreign Supplier Verification Program (FSVP). It’s an understandable misunderstanding: PCQI training covers hazard analysis, preventive controls, and risk-based decision-making—all core elements of FSVP.
- [What to Look For in an EHS Training Provider (And What Happens When You Choose Wrong)](https://www.registrarcorp.com/blog/food-beverage/food-beverage-regulations/what-to-look-for-ehs-training/): Many facilities believe their safety culture is solid until an incident reveals the cracks. Each year, organizations invest in workplace safety training that looks credible on paper but fails where it matters most: in the daily, high-pressure decisions of the workforce. The most significant operational failures aren’t usually caused by a lack of corporate intent; they are caused by relying on static training that was never engineered to drive real behavioral change or long-term retention.
- [Beyond the Fix: Using Training Systems to Eliminate Recordable Incidents](https://www.registrarcorp.com/blog/food-beverage/food-beverage-regulations/ehs-training-avoid-recordable-incidents/): When recordable incidents in the workplace occur, the first question a facility manager asks is rarely who made the mistake—it’s what system allowed it to happen. Most organizations are capable of fixing an immediate hazard, like a missing guardrail, a blocked exit, or a minor spill. However, those that successfully eliminate repeat incidents focus on fixing the training system that failed to prevent the incident in the first place. This systemic approach moves the organization away from blaming individuals and toward strengthening the institutional knowledge that protects everyone.
- [Workplace Safety Training: Protecting Productivity Through Operational Resilience](https://www.registrarcorp.com/blog/food-beverage/food-beverage-regulations/ehs-training-competitive-advantage/): Across regulated industries, workplace safety training is often viewed as a checklist item—a necessary obligation to keep operations running. However, industry leaders are shifting their perspective, treating foundational safety training as a performance multiplier rather than just another operational cost. They recognize that a safe environment is the bedrock of a high-performing culture, where employees can focus on excellence rather than basic survival.
- [Why Importers Choose Registrar for FSVP Training and Agent Coverage](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-training-and-agent-coverage/): Given our complex supply chain, many times we rely on foreign suppliers to provide us the unique ingredients needed for our finished products.  Most of these typical supplier verification activities become much more challenging when we have geographic distances, language barriers, competing country regulations, different time zones, etc.  It’s often helpful to work with importers who can help take responsibility for the food safety compliance of these foreign suppliers. But, even importers need support to successfully comply with the Foreign Supplier Verification Program (FSVP).  Where can importers go to get that support?
- [FSVP Records That Satisfy FDA: Examples and Templates for Audit-Ready Compliance](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-records-that-satisfy-fda/): When the FDA conducts an FSVP inspection, nearly every conclusion they reach comes down to one thing: your records. Not your intent, not your supplier’s assurances, not the strength of their HACCP plan alone—your documentation. Importers who understand what complete, compliant records look like stand in a far stronger position during FDA review.
- [Avoiding FDA Detention: FSVP Failures That Trigger Holds and Refusals](https://www.registrarcorp.com/blog/food-beverage/food-safety/fsvp-failures/): An FDA detention happens fast. One day your shipment is moving through customs; the next, it’s placed on hold because the FDA cannot confirm the safety of the product—or the adequacy of your verification program. What many importers don’t realize is that most detentions tied to FSVP are not caused by foreign supplier issues at all. They’re caused by gaps in the U.S. importer’s documentation.
- [The Ultimate FSVP Checklist: Records, Supplier Approval, and Verification Activities](https://www.registrarcorp.com/blog/food-beverage/food-safety/the-ultimate-fsvp-checklist/): Building or updating a Foreign Supplier Verification Program (FSVP) is not guesswork. The FDA’s expectations are precise, document-driven, and increasingly enforced. Whether you’re preparing for your first inspection or strengthening an existing program, a clear, structured checklist is one of the most valuable tools an importer can rely on.
- [FSVP 101: Who the “FSVP Importer” Is—and Who It Isn’t](https://www.registrarcorp.com/blog/food-beverage/food-safety/who-the-fsvp-importer-is/): Most companies importing food into the United States underestimate how costly it can be to misunderstand a single term in the Foreign Supplier Verification Program (FSVP). Few terms cause more confusion—or more enforcement issues—than the identity of the FSVP Importer. FDA investigators consistently report that facilities fail audits not because they lack documentation, but because the wrong party prepared it.
- [How to Build a HACCP Plan That Actually Works](https://www.registrarcorp.com/blog/food-beverage/food-safety/build-a-haccp-plan-that-works/): Most HACCP plans fail not because teams misunderstand the seven principles, but because their plans never made it out of the theoretical stage. They look complete on paper—flow diagrams, hazard tables, CCP decisions—but fall apart in audits because they don’t reflect how the process actually works. A HACCP plan that works is one that operators can follow, auditors can trust, and leadership can use to verify real control.
- [Why HACCP Still Matters—Even in a Preventive Controls Era](https://www.registrarcorp.com/blog/food-beverage/food-safety/haccp-and-preventive-controls/): Preventive controls have changed how facilities think about compliance, documentation, and regulatory oversight—but they have not replaced HACCP. Instead, they have made HACCP more important. Eevery detail analyzed by FDA reviewers and every requirement within SQF and other GFSI programs, still relies on the structure HACCP provides: validated limits, defensible hazard analysis, clear monitoring logic, and documentation that reflects real process control.
- [The New Normal for HACCP in 2026: Digital Records and FDA Alignment](https://www.registrarcorp.com/blog/food-beverage/food-safety/haccp-in-2026-digital-records/): HACCP hasn’t changed in principle, but everything around it has. The FDA’s modernization initiatives, the rise of digital documentation systems, and the increasing emphasis on real-time verification have reshaped what compliance looks like. In 2026, having a HACCP plan is no longer enough—your records, monitoring tools, and verification practices must be precise, accessible, and aligned with FDA expectations for transparency.
- [Top HACCP Audit Failures (and How to Prevent Them)](https://www.registrarcorp.com/blog/food-beverage/food-safety/top-haccp-audit-failures/): Most HACCP plans don’t fail because teams don’t understand the seven principles. They fail because small inconsistencies accumulate—gaps in monitoring, missing validation evidence, unclear hazard justification, or documentation that doesn’t match what actually happens on the floor. These issues rarely show up during internal reviews, but auditors catch them quickly.

## Blog Post Template Sections

## Media Coverage
- [Registrar Corp and U.S. Commercial Service Strengthen Partnership to Support Australian Companies Expanding into the U.S.](https://www.registrarcorp.com/media-coverages/press-release/australian-partnership-us-commercial-service/): SYDNEY--(BUSINESS WIRE)--Registrar Corp, the global leader in U.S. Food and Drug Administration (FDA) regulatory compliance services, partnered with the U.S. Commercial Service – Australia to host a high-level industry networking event at the U.S. Consulate General’s Residence in Sydney on May 14, 2026. The event convened Australian exporters, trade associations, and government representatives across FDA-regulated industries, reinforcing a shared commitment to enabling confident, compliant expansion into the U.S. market.
- [Insights from 2026 Global Food Safety Training Survey](https://www.registrarcorp.com/media-coverages/trade-publications/insights-from-2026-global-food-safety-training-survey/): Summary:New research has unveiled that top food manufacturers and facilities with superior training significantly outperform their counterparts in areas of food safety, compliance, productivity, employee engagement, and retention.
- [Q&A with David Lennarz, Co-Founder and President of Registrar Corp](https://www.registrarcorp.com/media-coverages/trade-publications/citybiz-qa-david-lennarz/): Summary: Baltimore’s CityBiz team interviews regional business leaders with global impact. Registrar Corp’s co-founder David Lennarz reviews how Registrar started with helping foreign countries comply with FDA food regulations into a much wider range of services to support compliance as an ongoing operating system for businesses in food and beverages, cosmetics, medical devices, and pharmaceutical industries.
- [Registrar Corp Releases Data and Insights from the 2026 Global Food Safety Training Survey](https://www.registrarcorp.com/media-coverages/press-release/registrar-corp-releases-data-and-insights-from-the-2026-global-food-safety-training-survey/): New research has unveiled that top food manufacturers and facilities with superior training significantly outperform their counterparts by implementing safer and more efficient operations. 
- [FDA Warning Letters Are Rising — What It Means for Food Companies](https://www.registrarcorp.com/media-coverages/trade-publications/fda-warning-letters-are-rising/): Summary: FDA warning letters to food manufacturers and importers are increasing as the agency shifts from education to sustained enforcement under FSMA. In this article for Food Manufacturing, Registrar Corp Director of Food Safety Fabiola Negron explains what’s driving the trend and what companies must do to avoid costly regulatory escalation.
- [How Modern Training Platforms Strengthen the Food Manufacturing Workforce](https://www.registrarcorp.com/media-coverages/trade-publications/how-modern-training-platforms-strengthen-the-food-manufacturing-workforce/): Summary:Food manufacturers are facing labor shortages, high turnover, and increasing regulatory complexity, pushing them to reevaluate their workforce training and development strategies. In an industry where safety, quality, and efficiency are of utmost importance, effective training has transcended compliance requirements and become a strategic advantage. 
- [How FSVP Audits Actually Work — And Where Importers Get Caught](https://www.registrarcorp.com/media-coverages/trade-publications/how-fsvp-audits-actually-work-2/): Overview: This article provides in-depth detail on what triggers an FSVP Audit, how the audit will unfold, how organization’s can be prepared for the audit, and how they can follow up.
- [Registrar Corp Acquires Dell Tech, Expanding Canadian Regulatory Expertise and Strengthening Global Market Access Solutions](https://www.registrarcorp.com/media-coverages/press-release/registrar-corp-acquires-dell-tech/): HAMPTON, Va. — Registrar Corp, the leading provider of regulatory compliance solutions for the food and beverage, medical device, cosmetic, and drug industries and a Paine Schwartz Partners portfolio company, announced its acquisition of Dell Tech, a Canada-based regulatory consulting firm known for its deep expertise in Canadian market requirements.
- [Sainsbury’s Partners with Registrar’s Foodsteps to Scale Supply Chain Emissions Tracking](https://www.registrarcorp.com/media-coverages/trade-publications/sainsburys-partners-with-registrars-foodsteps/): Overview: Sainsbury’s, the second-largest retailer in the United Kingdom with over 600 supermarkets and 850+ convenience stores, has partnered with Foodsteps (a Registrar Corp company) to improve supply chain emissions tracking. The collaboration focuses on product-level carbon data and supplier engagement. A new data ecosystem will support measurable decarbonization across food products. The partnership aims to improve transparency and resilience in the UK food system.
- [Costco’s $4.99 Rotisserie Chicken Is Facing 2 Class-Action Lawsuits](https://www.registrarcorp.com/media-coverages/trade-publications/costcos-4-99-rotisserie-chicken-is-facing-2-class-action-lawsuits/): Read full article here: https://www.foodandwine.com/costco-rotisserie-chicken-class-action-lawsuits-2026-11913657
- [Innovator Spotlight: Foodsteps Food Sustainability Company](https://www.registrarcorp.com/media-coverages/trade-publications/innovator-spotlight-foodsteps-food-sustainability-company/): Read full article here:https://www.foodbev.com/news/start-up-of-the-month-food-sustainability-company-foodsteps
- [Why the “Healthy” Label Deadline Is a Supply Chain Problem: A Q&A With David Lennarz of Registrar Corp](https://www.registrarcorp.com/media-coverages/trade-publications/why-the-healthy-label-deadline-is-a-supply-chain-problem-a-qa-with-david-lennarz-of-registrar-corp/): Read Article: https://foodindustryexecutive.com/2026/02/why-the-healthy-label-deadline-is-a-supply-chain-problem-a-qa-with-david-lennarz-of-registrar-corp/
- [FDA Watch Podcast: FDA’s 2026 Food Priorities](https://www.registrarcorp.com/media-coverages/trade-publications/fda-watch-podcast-fdas-2026-food-priorities/): Listen to the podcast: https://fdawatch.net/2026/02/09/fdas-2026-food-priorities/
- [2026 Year of ‘Clarity’ for US Beauty?](https://www.registrarcorp.com/media-coverages/trade-publications/2026-year-of-clarity-for-us-beauty/): Read full article here: https://insights.citeline.com/hbw-insight/beauty/business/2026-year-of-clarity-for-us-beauty-regulatory-reform-fda-enforcement-strategy-coming-into-focus-KQ5HVJ47YBE4LOJDLHRHLCRDEU/
- [Registrar Corp Acquires TechniCAL and Becomes the Global Compliance Leader in Shelf-stable Packaged Foods Safety](https://www.registrarcorp.com/media-coverages/press-release/registrar-corp-acquires-technical/): Registrar Corp Becomes the Global Compliance Leader in Shelf-stable Packaged Foods Safety
- [Rates, Raw Materials, and Risk: Economic Considerations for Food Manufacturers in 2026](https://www.registrarcorp.com/media-coverages/trade-publications/rates-raw-materials-and-risk-economic-considerations-for-food-manufacturers-in-2026/): This article argues that 2026 will be a year of managed uncertainty rather than crisis or boom for food manufacturers. Interest rates are expected to ease somewhat but remain structurally higher than the pre-COVID era, meaning capital will still require discipline and strong justification. Raw material costs may stabilize or soften in some categories, but volatility will persist due to weather, geopolitics, and supply constraints, making predictability and risk management more important than chasing short-term price relief. Consumer behavior is expected to stay value-focused, limiting pricing power even as input and compliance costs continue to rise.
- [FDA’s FSMA 204 Rule Change. Now What?](https://www.registrarcorp.com/media-coverages/trade-publications/fdas-fsma-204-rule-change-now-what/): Read full article here: https://www.foodlogistics.com/safety-security/food-safety/article/22957035/registrar-corp-fdas-fsma-204-rule-change-now-what
- [Registrar Corp Acquires CMC Medical Devices to Make Global Compliance Quick and Easy](https://www.registrarcorp.com/media-coverages/press-release/registrar-corp-acquires-cmc-medical-devices/): -- (BUSINESS WIRE) -- Registrar Corp, a global leader in regulatory compliance and technology solutions and a Paine Schwartz Partners portfolio company, today announced the acquisition of CMC Medical Devices (CMC), a Spain-based provider of medical device regulatory, clinical, and compliance consulting services. The combination of Registrar Corp’s global network and CMC’s clinical and technical expertise creates a unified partner to help medical device and in vitro diagnostic (IVD) manufacturers bring products to market faster and with greater confidence.
- [The Cost of FSVP Non-Compliance](https://www.registrarcorp.com/media-coverages/trade-publications/fsvp-non-compliance/): The Foreign Supplier Verification Program (FSVP) is a cornerstone of the FDA’s Food Safety Modernization Act (FSMA), designed to uphold the safety of imported food products. This trade publication delves into the significant implications of FSVP non-compliance, from financial and reputational risks to operational disruptions. It also highlights common pitfalls businesses face when navigating the complexities of compliance.
- [FSVP’s Impact on Canadian Suppliers](https://www.registrarcorp.com/media-coverages/trade-publications/fsvp-canadian-suppliers/): Canadian suppliers are highlighted with information on their obligations under FSSRA with the FDA including documentation requirements and compliance protocols. It also looks at scenarios where full FSVP requirements apply to Canadian suppliers and what evidence US importers need to see to verify compliance – food safety plans, audit reports and certificates of analysis.
- [Registrar Corp Acquires Personal Care Regulatory (PCR), Expanding Global Cosmetic Regulatory Compliance Services ](https://www.registrarcorp.com/media-coverages/press-release/registrar-acquires-pcr/): – Registrar Corp, the world’s largest cosmetics compliance company, is pleased to announce its acquisition of Personal Care Regulatory (PCR) Group, a leading cosmetic regulatory, toxicology, and compliance company based in the United Kingdom (UK) and Ireland. This strategic acquisition extends Registrar’s global regulatory compliance capabilities.
- [Cosmetic Industry Faces Significant Non-Compliance Under New FDA Regulations ](https://www.registrarcorp.com/media-coverages/press-release/48-mocra-non-compliant/): Discover why 48% of companies selling imported cosmetics at America’s top 25 retailers are non-compliant with MoCRA.
- [AEM Streamlines Adverse Event Reporting Process](https://www.registrarcorp.com/media-coverages/trade-publications/aem-streamlines-adverse-effect-reporting-process/): Registrar Corp. has introduced an Adverse Event Management (AEM) software in response to the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). This new regulation mandates that cosmetic brands include contact information on both primary and secondary packaging for reporting adverse events. The software provides companies with a brand-specific URL or QR code, enabling consumers to report issues directly to the brand instead of going to the FDA.
- [How MoCRA Compliance & AEM Software Transforms Reporting](https://www.registrarcorp.com/media-coverages/trade-publications/how-mocra-compliance-and-aem-software-are-transforming-cosmetics-industry-reporting/): The article focuses on the impact of the Modernization of Cosmetics Regulation Act (MoCRA) on the cosmetics industry, emphasizing the shift toward improved adverse event reporting and our new AEM Software. The new regulation, which came into effect at the end of 2023, requires cosmetic companies to enhance transparency by listing contact information on packaging for consumers to report any adverse effects. This significant change requires companies to track, evaluate, and report these events to the FDA, adding a layer of accountability.
- [Introducing AEM: A MoCRA-Assist Software Package](https://www.registrarcorp.com/media-coverages/trade-publications/registrar-corp-launches-mocra-assist-software-package/): Introducing AEM, (Adverse Event Management software), a first-of-its-kind platform designed to help cosmetics companies comply with the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). The software securely collects sensitive data, tracks adverse events globally, and formats serious cases for FDA submission in the MedWatch format. MoCRA’s complex reporting requires coordination across various departments, including compliance, marketing, legal, and R&D. AEM addresses this need by streamlining real-time data processing and investigation to meet the 15-day reporting requirement.
- [Cosmetic Industry Not Prepared For New Adverse Event Rules](https://www.registrarcorp.com/media-coverages/trade-publications/registrar-corp-sees-software-helping-cosmetics-industry-not-prepared-for-new-fda-adverse-event-reporting-requirements/): Registrar Corp has introduced its Adverse Event Management (AEM) software to aid the cosmetic industry in complying with the FDA’s Modernization of Cosmetics Regulation Act (MoCRA). MoCRA introduces stricter requirements for cosmetic product safety, including displaying contact information on packaging, collecting consumer medical data, and reporting serious adverse events to the FDA within 15 days. Previously, these measures were voluntary, but now they are mandatory, requiring coordination between various departments like marketing, legal, quality assurance, and R&D.
- [Meeting 5 MoCRA Mandates for Adverse Event Reporting](https://www.registrarcorp.com/media-coverages/trade-publications/meeting-5-mocra-mandates-for-adverse-event-reporting-registrar-corp-launches-new-tool/): Registrar Corp has launched its Adverse Event Management (AEM) software to assist cosmetics companies in meeting the FDA’s new requirements MoCRA mandates. These mandates include displaying contact information on packaging, collecting detailed consumer medical data, investigating adverse events, reporting serious cases to the FDA within 15 days, and maintaining records for up to six years.
- [FDA Implementing New Rules Governing Cosmetics](https://www.registrarcorp.com/media-coverages/video-interview/fda-implementing-new-rules-governing-makeup-cosmetics-what-to-know/): Under MoCRA, federal government has introduced new safety regulations for cosmetic labels, representing the most significant FDA updates in 85 years. These changes focus on three main aspects: professional-use makeup, complaint reporting labels, and fragrance allergen labeling.
- [FDA MoCRA Requirements Could Lead to Changes in Makeup](https://www.registrarcorp.com/media-coverages/video-interview/new-fda-requirements-could-lead-to-changes-in-makeup/): The federal government has rolled out new MoCRA requirements aimed at improving cosmetic safety, marking the most substantial FDA changes to cosmetic legislation  in 85 years. These updates focus on three critical areas:
- [FDA MoCRA Rules Change the Way Cosmetic Brands Do Business](https://www.registrarcorp.com/media-coverages/video-interview/new-fda-rules-change-the-way-cosmetic-brands-do-business/): The FDA has introduced new MoCRA rules that will affect various aspects of cosmetics, including those found in your medicine cabinet, shower routine, and skincare products. These rules represent a significant shift for cosmetic companies, who will now have to comply with more stringent requirements. According to David Lennarz, co-founder and president of Registrar Corp., these changes are long overdue, as the cosmetics industry has only faced voluntary guidelines since the Food, Drug, and Cosmetic Act of 1938.
- [MoCRA Changes to the Cosmetic Industry](https://www.registrarcorp.com/media-coverages/video-interview/fda-changes-to-the-cosmetic-industry/): In this video, Jaclyn Bellomo, Director of Cosmetic Science and Regulatory Affairs at Registrar Corp., discusses the significant changes introduced by the Modernization of Cosmetics Regulation Act (MoCRA). As the most extensive update to cosmetics regulations in over 80 years, MoCRA brings new requirements aimed at enhancing consumer safety and increasing transparency within the cosmetics industry.
- [How MoCRA Will Change Your Favorite Cosmetic Brand](https://www.registrarcorp.com/media-coverages/video-interview/changes-you-could-see-to-your-favorite-cosmetic-brands/): In this video, David Lennarz, President of Business Development and Operations at Registrar Corp., discusses the FDA’s new MoCRA adverse event regulations. The updated rules aim to enhance consumer safety and transparency in the cosmetics industry.
- [Cosmetics Industry Not Prepared for FDA’s New Adverse Events Reporting Requirements](https://www.registrarcorp.com/media-coverages/press-release/adverse-event-management-launch/): Hampton, Va., July 23, 2024 — Registrar Corp, the world’s largest FDA compliance company with 32,000 clients in 190 countries, announced today the launch of Adverse Event Management (AEM) Software.  The first-of-its-kind software enables cosmetics companies to comply with the U.S. Food and Drug Administration’s (FDA) Modernization of Cosmetics Regulation Act (MoCRA).
- [Registrar Corp acquires Foodsteps as food industry faces mounting pressures to deliver supply chain sustainability](https://www.registrarcorp.com/media-coverage/foodsteps-aqcuisition/): July 23, 2024, Registrar Corp (“Registrar”), a Paine Schwartz Partners portfolio company and the U.S.’ leading provider of regulatory and compliance software for food, cosmetic, and life science companies, has acquired Foodsteps, a pioneering UK-based company dedicated to helping food businesses reduce the environmental impact of their products. 
- [Elevating Data Security: Registrar Corp’s Landmark ISO 27001 Certification](https://www.registrarcorp.com/press/elevating-data-security-registrar-corps-landmark-iso-27001-certification/): HAMPTON, Va., May 8, 2024 /CISION/ — Registrar Corp, the leader in U.S. Food and Drug Administration (FDA) registration and compliance, proudly announces its achievement of the prestigious ISO 27001 certification, marking a significant milestone in the company’s ongoing commitment to data security and protection. Serving over 30,000 companies across more than 190 countries, Registrar Corp has solidified its reputation as the trusted partner for FDA compliance and regulatory requirements, keeping the confidentiality and integrity of proprietary customer information in the food and beverage, cosmetic, medical device, and drug industries.
- [U.S. Food Importers Can Now Meet Tough FSVP Compliance Requirements with ComplyHub](https://www.registrarcorp.com/press/us-food-importers-can-meet-fsvp-requirements-with-complyhub/): New FSVP compliance software ComplyHub helps U.S. food importers monitor suppliers, manage documents, and boost business growth.
- [FDA Has Officially Opened the Cosmetic Portal to Industry ](https://www.registrarcorp.com/press/cosmetic-portal/): World’s largest FDA compliance company is ready on day one, already serving the needs of hundreds. 
- [Registrar Corp Appoints Raj Shah As Chief Executive Officer](https://www.registrarcorp.com/press/raj-shah/): World’s Largest FDA Compliance Software Firm Positioned to Meet Demand from New Cosmetics Industry Regulation with Expanded Capabilities.
- [Leading FDA Compliance Specialist Offers Cosmetic Companies a Simpler Way to Manage Adverse Event Reporting Requirements](https://www.registrarcorp.com/press/cosmetic-adverse-events-pr/): New Adverse Event Reporting software and services help save cosmetic companies time and effort in complying with updated FDA regulations.
- [MoCRA Wizard From Registrar Corp Helps You Understand Your Company’s Responsibilities Under New FDA Cosmetic Regulations](https://www.registrarcorp.com/media-coverages/press-release/mocra-wizard/): Introducing MoCRA Wizard, the newest tool from Registrar Corp to quickly understand your responsibilities under MoCRA

## Compliance Trainings
- [PCQI 2.0 Training & Certificate — FSPCA Approved](https://www.registrarcorp.com/compliance-training/food-beverage/pcqi-training/): Get FDA-compliant PCQI training—100% self-paced, FSPCA-recognized, and trusted by 30k+ professionals. Gain real-world skills with a satisfaction guarantee.
- [SQF 10 Practitioner Training & Implementation Program](https://www.registrarcorp.com/compliance-training/food-beverage/sqf-practitioner/): Learn how to manage your SQF Food Safety and Quality Program with Registrar Corp’s 100% online SQF Training. Earn a Certificate of Completion today.
- [Online HACCP Certification & Training](https://www.registrarcorp.com/compliance-training/food-beverage/haccp-certification/): Get HACCP certified with 100% self-paced training trusted by 30k+ professionals. Strengthen compliance, avoid audit risk, and learn with a satisfaction guarantee.
- [FSVP Training: FSPCA Foreign Supplier Verification Programs](https://www.registrarcorp.com/compliance-training/food-beverage/fsvp-online-training-fspca-foreign-supplier-verification-programs/): Master FSVP with 100% self-paced, FDA-aligned training trusted by 30k+ professionals. Build confidence, reduce risk, and get your certificate—guaranteed.
- [Animal Food PCQI Online Training: FSPCA Preventive Controls for Animal Food](https://www.registrarcorp.com/compliance-training/food-beverage/animal-food-pcqi-online-training-fspca-preventive-controls-for-animal-food/): Become a trained animal food PCQI & earn your official FSPCA PCQI Certificate. Learn to write your Food Safety Plan with our 5-Star rated, self-paced course.
- [Complete Training Package for FSSC 22000](https://www.registrarcorp.com/compliance-training/food-beverage/complete-training-package-for-fssc-22000/): Learn about the requirements of FSSC 22000 and how to build, document, and audit an FSSC 22000 food safety system. 100% Online, 5-Star Course.
- [Better Process Control School for Retort Foods](https://www.registrarcorp.com/compliance-training/food-beverage/better-process-control-school-retort-certification-course/): Earn BPCS Retort Certification with curriculum approved by the FDA. Learn retort operations, thermal processing, and food safety in this self-paced BPCS course.
- [Better Process Control School for Acidified Foods](https://www.registrarcorp.com/compliance-training/food-beverage/better-process-control-school-acidified-foods/): Earn BPCS certification with curriculum approved by the FDA with our online Better Process Control School. Learn acidified foods food safety, thermal processing, and compliance.
- [BPCS Full Certification Bundle: Acidified, Retort, Aseptic](https://www.registrarcorp.com/compliance-training/food-beverage/bpcs-full-certification-bundle/): Earn your certification covering retort, acidified and aseptic food processing. Meet FDA and USDA requirements for your facility and advance your career with our 100% online Better Process Control School training.
- [Better Process Control School for Aseptic Foods](https://www.registrarcorp.com/compliance-training/food-beverage/better-process-control-school-aseptic-foods/): Earn BPCS Aseptic Certification with curriculum approved by the FDA in this BPCS course from Registrar. 100% online, self-paced aseptic processing and packaging training.
- [BPCS Retort + Acidified Food Certification Package 
](https://www.registrarcorp.com/compliance-training/food-beverage/better-process-control-school-retort-acidified-foods-certification-course-package/): Earn your retort and acidified foods certification with our expert-led thermal processing course. Complete online training for Better Process Control compliance.
- [Transition Course: Updating to SQF Edition 10](https://www.registrarcorp.com/compliance-training/food-beverage/sqf-edition-10-conversion-course/): Update your facility with this SQF Edition 10 Conversion Course for fast implementation of new code requirements.
- [Retort Operator Training – Steam Retorts](https://www.registrarcorp.com/compliance-training/food-beverage/retort-operator-training-steam/): Self-paced online steam retort operator training covering retort basics, cycle operation, records, and deviation handling.
- [Retort Operator Training – Steam-Air](https://www.registrarcorp.com/compliance-training/food-beverage/retort-operator-training-steam-air/): Self-paced training for steam-air retort operators: core retort fundamentals, steam-air cycle operation, records, and deviation response.
- [Retort Operator Training – Water Spray Retorts (Static)](https://www.registrarcorp.com/compliance-training/food-beverage/retort-operator-water-spray-static/): Self-paced training for static water spray retort operators: fundamentals, cycle operation, records, and deviation handling.
- [Retort Operator Training – Water Spray Retorts (Rotary)](https://www.registrarcorp.com/compliance-training/food-beverage/retort-operator-water-spray-rotary/): Self-paced training for rotary water spray retort operators: core retort fundamentals, rotary cycle operation, records, and deviation response.
- [Retort Operator Training – Water Immersion (Rotary)](https://www.registrarcorp.com/compliance-training/food-beverage/retort-operator-water-immersion-rotary/): Self-paced training for rotary water immersion retort operators: core retort fundamentals, immersion rotary cycle operation, records, and deviation response.
- [BRCGS Issue 9 Complete Training Program](https://www.registrarcorp.com/compliance-training/food-beverage/brcgs-issue-9-complete-training-package/): Learn how to manage your BRCGS food safety program with Registrar Corp’s 100% online BRC Training. Earn a Certificate of Completion today.
- [Complete Training Package for ISO 22000:2018](https://www.registrarcorp.com/compliance-training/food-beverage/complete-training-package-for-iso-220002018/): Lead your company to ISO 22000 certification! Self-paced, online course teaches ISO 22000:2018 implementation, documentation and internal auditing.
- [HACCP + PCQI Training Package](https://www.registrarcorp.com/compliance-training/food-beverage/haccp-pcqi-training-package/): Gain HACCP Certification and your PCQI Certificate with this 100% online and self-paced compliance training bundle.
- [SQF Practitioner Training + HACCP Certification Bundle](https://www.registrarcorp.com/compliance-training/food-beverage/sqf-sqf-haccp/): Affordable HACCP & SQF Training: 5-star online course to equip SQF Practitioners with essential skills and compliance expertise. Start anytime.
- [Internal Auditing for SQF 10](https://www.registrarcorp.com/compliance-training/food-beverage/sqf-internal-auditor-training/): Become proficient in SQF internal auditing with our online SQF Internal Auditor Training. Includes mock audits, templates & support.
- [BRCGS Internal Auditor Training](https://www.registrarcorp.com/compliance-training/food-beverage/brcgs-internal-auditor-training/): Become a BRCGS Internal Auditor. Gain the qualifications and skills you need in order to audit your company’s BRCGS system effectively and with confidence.
- [FSSC 22000 Version 6 Internal Auditor Training](https://www.registrarcorp.com/compliance-training/food-beverage/fssc-22000-internal-auditor-training/): Gain the qualifications and skills you need to audit your company’s FSSC 22000 system effectively and with confidence.
- [ISO 22000 Internal Auditor Training](https://www.registrarcorp.com/compliance-training/food-beverage/iso-22000-internal-auditor-training/): Learn to set up an ISO 22000 internal audit program and conduct internal audits. Includes interactive practice audit. Self-paced course - start today!
- [ISO 9001:2015 Internal Auditor Training](https://www.registrarcorp.com/compliance-training/food-beverage/iso-90012015-internal-auditor/): Train new ISO 9001:2015 internal auditors on the principles of auditing and the requirements for an internal audit program.
- [HACCP Foundations](https://www.registrarcorp.com/compliance-training/food-beverage/foundations-of-haccp/): Learn the basics of HACCP including Foundations, Principles of HACCP, Prerequisite Programs, and Preliminary Steps in developing a HACCP Plan.
- [Understanding the SQF 10 Code](https://www.registrarcorp.com/compliance-training/food-beverage/mastering-sqf/): Learn SQF Edition 10 requirements, Food Safety Management Systems, GMPs, and compliance steps. Ideal for management and Food Safety teams.
- [Understanding FSSC 22000 Training](https://www.registrarcorp.com/compliance-training/food-beverage/understanding-fssc-22000/): What is FSSC 22000 and what does it mean for you? Get an introduction to the requirements of FSSC 22000 in user-friendly self-paced training.
- [Juice HACCP Plan Development Training](https://www.registrarcorp.com/compliance-training/food-beverage/juice-haccp-plan-development/): Get your Juice HACCP Certification with our user-friendly, self-paced compliance training. Includes the official HACCP Alliance certificate.
- [FSMA Allergens Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/allergens/): Avoid a common cause of product recalls. Learn about FSMA allergen requirements in this 100% online, self-paced course.
- [FDA Regulated Imports & Importing to the US: Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/imports/): Learn the basics of importing food, acts and regulations, entry process, inspection, investigation, compliance and enforcement actions, and import fraud.
- [Labeling for Food Manufacturers: Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/labeling-for-food-manufacturers/): Gain in depth insight and understanding of FDA’s Food Labeling Regulations with our compliance training created by industry experts.
- [Food Labeling for Regulators: A Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/labeling-for-regulators/): Compliance with FDA labeling requirements for food products is essential. Learn the basics of labeling laws and regulations.
- [Preventive Controls Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/preventive-controls/): Learn the basics of food safety plans and preventive controls implemented by FDA compliant feed and food manufacturing facilities.
- [Pest Control Training](https://www.registrarcorp.com/compliance-training/food-beverage/pest-control/): An effective pest control program is an essential part of a firm’s sanitary operations. Learn to control pests in your food production facility.
- [FDA & Food Product Recalls: Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/recalls/): It is important to know how to handle food recalls and be prepared if one becomes necessary. Learn how to remove a product from commerce.
- [Sanitation Operator Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/sanitation-operator/): Learn basic sanitation operator principles, and the importance of cleaning and sanitizing food manufacturing production lines, equipment, and facilities.
- [Food Facility Sanitation Practices: Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/sanitation-practices/): Learn how to meet FDA compliance with this sanitation practices course created by by top experts in the industry.
- [Food Transportation Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/transportation/): Learn the foundations of transportation of food and ingredients, transportation methods, inspections, security, and product safety.
- [Food Traceability Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/traceability/): Explore the foundations of food traceability, supply chain management, documentation, communication, and technology in the food industry.
- [Listeria Control Specialist Certificate Program](https://www.registrarcorp.com/compliance-training/food-beverage/listeria-control-specialist/): Protect your facility from Listeria and related recalls. Become a formally recognized Listeria Control Specialist with our online certification program.
- [GMPs in Food Manufacturing Facilities to Control Listeria](https://www.registrarcorp.com/compliance-training/food-beverage/gmps-listeria/): Learn the critical role of GMPs in managing and mitigating risks associated with Listeria monocytogenes (Lm) in food production facilities.
- [Prevention & Control of Listeria in Freezer Systems and Equipment](https://www.registrarcorp.com/compliance-training/food-beverage/prevention-and-control-of-listeria-in-freezer-systems-and-equipment/): Learn the critical skillsets required to prevent and control Listeria in freezer systems and maintain FDA compliance throughout your process.
- [Hygienic Facility & Equipment Design for Food Manufacturing Facilities](https://www.registrarcorp.com/compliance-training/food-beverage/hygienic-facility-and-equipment-design-for-food-manufacturing-facilities/): Learn what it takes to maintain FDA Compliance with food facility sanitation regulations regarding hygienic facility and equipment design.
- [Environmental Monitoring for Listeria: Compliance Training](https://www.registrarcorp.com/compliance-training/food-beverage/environmental-monitoring/): Learn about environmental monitoring for listeria including environmental sampling, testing methods, root cause analysis, and corrective actions.
- [Hygienic Zoning for Food Manufacturing Facilities](https://www.registrarcorp.com/compliance-training/food-beverage/hygienic-zoning-for-food-manufacturing-facilities/): Master the principles of Hygienic Zoning with our compliance training course created by top experts in the industry.
- [Sanitation Controls for Food Manufacturing Facilities](https://www.registrarcorp.com/compliance-training/food-beverage/sanitation-controls/): Learn to identify, plan for, and manage Listeria and other pathogens in your food facilities by leveraging the tools for sanitation controls.
- [ISO 22000 Templates for Manual & Procedure](https://www.registrarcorp.com/compliance-training/food-beverage/iso-220002018-manual-procedure-templates/): Download ready-to-edit Manual and Procedures to design and document your ISO 22000 templates for Food Safety Management Systems.
- [Templates & Tools for SQF 10](https://www.registrarcorp.com/compliance-training/food-beverage/sqf-template-package/): Simplify implementation of your SQF System with this package of over 50 procedure templates, form templates, and GMP tables. The templates are downloadable and easy for you to customize to your facility.