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Filing a DMF for Delrin (R) Acetal Resin with the U.S. FDA

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

  - Dupont Engineering Polymers

Registrar Corp can help you to properly prepare and submit your Delrin (R) Acetal Resin DMF to FDA.

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

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

For more information about filing a DMF for Delrin (R) Acetal Resin, 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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