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Filing a DMF for Terluran GP-22natural with the U.S. FDA

Filing a drug master file (DMF) for Terluran GP-22natural can be a useful mechanism to market your Terluran GP-22natural to the U.S. Drug Industry. Typical Terluran GP-22natural producers who have filed a DMF for Terluran GP-22natural include:

  - BASF Aktiengesellschaft

Registrar Corp can help you to properly prepare and submit your Terluran GP-22natural DMF to FDA.

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

  - Format, assemble and deliver your Terluran GP-22natural DMF to FDA
  - Submit letters of authorization regarding your Terluran GP-22natural to FDA
 - Provide changes, additions and maintenance of your Terluran GP-22natural DMF
  - Respond to issues relating to ownership of your Terluran GP-22natural DMF
  - Assist with submission of responses to FDA concerning your Terluran GP-22natural DMF
  - Perform any required annual updates for your Terluran GP-22natural DMF

For more information about filing a DMF for Terluran GP-22natural, 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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