Registrar Corp

HomeDrugsDrug Master Files (DMF)DMF ExamplesType IV DMFs › U.S. FDA Certiseal FC-300 Regulations

Filing a DMF for Certiseal FC-300 with the U.S. FDA

Filing a drug master file (DMF) for Certiseal FC-300 can be a useful mechanism to market your Certiseal FC-300 to the U.S. Drug Industry. Typical Certiseal FC-300 producers who have filed a DMF for Certiseal FC-300 include:

  - Mantrose Haeuser Co Inc

Registrar Corp can help you to properly prepare and submit your Certiseal FC-300 DMF to FDA.

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

  - Format, assemble and deliver your Certiseal FC-300 DMF to FDA
  - Submit letters of authorization regarding your Certiseal FC-300 to FDA
 - Provide changes, additions and maintenance of your Certiseal FC-300 DMF
  - Respond to issues relating to ownership of your Certiseal FC-300 DMF
  - Assist with submission of responses to FDA concerning your Certiseal FC-300 DMF
  - Perform any required annual updates for your Certiseal FC-300 DMF

For more information about filing a DMF for Certiseal FC-300, 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