Registrar Corp

HomeDrugsDrug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA PVC Film Regulations

Filing a DMF for PVC Film with the U.S. FDA

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

  - Ineos Films Gmbh
  - AC Folien Gmbh

Registrar Corp can help you to properly prepare and submit your PVC Film DMF to FDA.

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

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

For more information about filing a DMF for PVC Film, 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