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Filing a DMF for TD-2B Adhesive with the U.S. FDA

Filing a drug master file (DMF) for TD-2B Adhesive can be a useful mechanism to market your TD-2B Adhesive to the U.S. Drug Industry. Typical TD-2B Adhesive producers who have filed a DMF for TD-2B Adhesive include:

  - Adhesives Research Inc

Registrar Corp can help you to properly prepare and submit your TD-2B Adhesive DMF to FDA.

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

  - Format, assemble and deliver your TD-2B Adhesive DMF to FDA
  - Submit letters of authorization regarding your TD-2B Adhesive to FDA
 - Provide changes, additions and maintenance of your TD-2B Adhesive DMF
  - Respond to issues relating to ownership of your TD-2B Adhesive DMF
  - Assist with submission of responses to FDA concerning your TD-2B Adhesive DMF
  - Perform any required annual updates for your TD-2B Adhesive DMF

For more information about filing a DMF for TD-2B Adhesive, 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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