Registrar Corp

HomeDrugsDrug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA Disposable Syringe System Regulations

Filing a DMF for Disposable Syringe System with the U.S. FDA

Filing a drug master file (DMF) for Disposable Syringe System can be a useful mechanism to market your Disposable Syringe System to the U.S. Drug Industry. Typical Disposable Syringe System producers who have filed a DMF for Disposable Syringe System include:

  - Gerresheimer Bunde Gmbh

Registrar Corp can help you to properly prepare and submit your Disposable Syringe System DMF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Format, assemble and deliver your Disposable Syringe System DMF to FDA
  - Submit letters of authorization regarding your Disposable Syringe System to FDA
 - Provide changes, additions and maintenance of your Disposable Syringe System DMF
  - Respond to issues relating to ownership of your Disposable Syringe System DMF
  - Assist with submission of responses to FDA concerning your Disposable Syringe System DMF
  - Perform any required annual updates for your Disposable Syringe System DMF

For more information about filing a DMF for Disposable Syringe System, simply click below:




Live Help

 
U.S. FDA Regulations:

U.S. FDA DMF Regulation: 21 C.F.R. Section 314.420


Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
Home | About Us | News | Resources | Exhibitions | Seminars | Associations | Careers | Sitemap | Terms of Use © 2014 Registrar Corp
 
Food and Beverages | Drugs | Cosmetics | Medical Devices | Radiation-Emitting Electronic Devices | Color Additives | Tobacco