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

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

  - Georgia Gulf Corp

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

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

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

For more information about filing a DMF for PVC Resins, simply click below:




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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.
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