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Filing a DMF for Blister Foil with the U.S. FDA

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

  - Aluflexpack D O O

Registrar Corp can help you to properly prepare and submit your Blister Foil DMF to FDA.

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

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

For more information about filing a DMF for Blister Foil, 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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