Category: Cosmetics

Expert Jaclyn Bellomo will take you through an introduction to the FDA’s expanded authority and regulatory power concerning Adverse Events in cosmetics. This new requirement will significantly impact how companies handle health-related consumer reports, as the FDA can request records if there is a reasonable probability of causing a serious adverse health consequence or public

With sustainability and innovation on one side and rapidly shifting consumer behavior on the other, the Beauty and Cosmetics industry is experiencing a profound transformation. Companies are working to meet these demands while also navigating evolving regulatory requirements.   This webinar will delve into the critical trends shaping the future of Beauty and Cosmetics packaging and

FDA has expanded authority and regulatory power specifically for Adverse Events. FDA can now issue a Mandatory Recall if they determine that a cosmetic product is adulterated or that the exposure will cause serious adverse health consequences. They can also suspend a facility if there is reasonable probability of causing a serious adverse health consequence

Booth 871 

Booth Number: 562  

This webinar will take you through an introduction of the requirements of 21 CFR 58, Good Laboratory Practices for Nonclinical Studies and give you valuable examples of why GLP is important in a lab setting while identifying if the regulation applies to you and your company. We will also give you key strategies for implementation

Você sabia que dois dos motivos mais comuns pelos quais os produtos alimentícios são proibidos de entrar nos EUA, são erros de rotulagem e aditivos alimentares ilegais? Muitas empresas não descobrem que seus produtos não são permitidos no mercado dos EUA até que seja tarde demais, e eles são detidos no porto. Qualquer empresa que

Learn about the upcoming labeling requirements mandated by MoCRA as well as the general requirements all cosmetic products must meet. We describe in detail what must appear on your products’ labels and the timelines for compliance. 

Mit dem bevorstehenden Inkrafttreten des MoCRA am 1. Juli war es noch nie so wichtig wie heute, die neuen Vorschriften der US-amerikanischen FDA für die Kosmetikindustrie nachzu-kommen und unterhalten. Nehmen Sie an ” Praktische Schritte, um schnell MoCRA-konform zu werden ” teil, in dem wir Kosmetikmarken und -hersteller mit Wissen und Strategien ausstatten werden, um

Tenuto conto dell’avvicinarsi della fine del periodo di “discrezionalità applicativa” decretata dalla FDA al 1° luglio prossimo, essere e rimanere in regola con i nuovi requisiti per la cosmetica diventa urgente. Partecipate al nostro webinar “Passi pratici per adeguarsi rapidamente al MoCRA” per acquisire le informazioni necessarie all’adeguamento normativo e alla definizione delle vostre strategie

Booth Number: 518

This webinar conducted by Registrar Corp with our cosmetic expert, Jaclyn Bellomo, shares key provisions of MoCRA that you must follow and provides insight into how they impact your business operations. Dive into the various challenges with product listings, navigating Cosmetics Direct, new adverse event requirements, and more.

Booth Number: D27

This webinar conducted by Registrar Corp and Amazon will provide businesses seeking U.S. expansion insights on navigating new FDA requirements enacted under the Modernization of Cosmetics Regulation Act (MoCRA) and will cover best practices for cross-border e-commerce solutions.

Our team will attend PCPC Legal & Regulatory Day 2024.

Jaclyn Bellomo, Director of Cosmetic Science & Regulatory Affairs, will share “MoCRA Explained: Understanding New FDA Cosmetic Regulations” on April 23, at 2:30PM ET.

In this webinar, we unmask the complexities behind the booming “clean beauty” trend and discuss the regulatory and legal pitfalls to avoid.