Registrar Corp

HomeDrugsDrug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA Polyethylene Resins Regulations

Filing a DMF for Polyethylene Resins with the U.S. FDA

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

  - Nova Chemicals Ltd
  - Huntsman Polymers Corporation

Registrar Corp can help you to properly prepare and submit your Polyethylene Resins DMF to FDA.

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

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

For more information about filing a DMF for Polyethylene Resins, 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