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Filing a DMF for Desiccant Packaging with the U.S. FDA

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

  - Aridien Incorporated

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

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

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

For more information about filing a DMF for Desiccant Packaging, 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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