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Filing a DMF for Chitosan (Trade Name Protasan(Tm)) with the U.S. FDA

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

  - FMC Biopolymer As

Registrar Corp can help you to properly prepare and submit your Chitosan (Trade Name Protasan(Tm)) DMF to FDA.

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

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

For more information about filing a DMF for Chitosan (Trade Name Protasan(Tm)), 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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