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Filing a DMF for Tablet Containers with the U.S. FDA

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

  - Promens Sa

Registrar Corp can help you to properly prepare and submit your Tablet Containers DMF to FDA.

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

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

For more information about filing a DMF for Tablet Containers, 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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