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Filing a DMF for Cap Liners with the U.S. FDA

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

  - Selig Sealing Products Inc

Registrar Corp can help you to properly prepare and submit your Cap Liners DMF to FDA.

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

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

For more information about filing a DMF for Cap Liners, 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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