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Filing a DMF for Aerosil with the U.S. FDA

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

  - Evonik Degussa Corporation

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

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

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

For more information about filing a DMF for Aerosil, 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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