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Filing a DMF for Adhesive Formulations with the U.S. FDA

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

  - Rohm and Haas Co

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

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

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

For more information about filing a DMF for Adhesive Formulations, 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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