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Filing a DMF for Dry Keep Desiccant with the U.S. FDA

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

  - Tricorbraun

Registrar Corp can help you to properly prepare and submit your Dry Keep Desiccant DMF to FDA.

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

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

For more information about filing a DMF for Dry Keep Desiccant, 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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