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Filing a DMF for MPE953M-1 with the U.S. FDA

Filing a drug master file (DMF) for MPE953M-1 can be a useful mechanism to market your MPE953M-1 to the U.S. Drug Industry. Typical MPE953M-1 producers who have filed a DMF for MPE953M-1 include:

  - Sonoco Flexible Packaging

Registrar Corp can help you to properly prepare and submit your MPE953M-1 DMF to FDA.

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

  - Format, assemble and deliver your MPE953M-1 DMF to FDA
  - Submit letters of authorization regarding your MPE953M-1 to FDA
 - Provide changes, additions and maintenance of your MPE953M-1 DMF
  - Respond to issues relating to ownership of your MPE953M-1 DMF
  - Assist with submission of responses to FDA concerning your MPE953M-1 DMF
  - Perform any required annual updates for your MPE953M-1 DMF

For more information about filing a DMF for MPE953M-1, 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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