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Filing a DMF for Acrylic Adhesive Emulsions with the U.S. FDA

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

  - Rohm and Haas Co

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

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

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

For more information about filing a DMF for Acrylic Adhesive Emulsions, 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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