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Filing a DMF for HY-10 Adhesive with the U.S. FDA

Filing a drug master file (DMF) for HY-10 Adhesive can be a useful mechanism to market your HY-10 Adhesive to the U.S. Drug Industry. Typical HY-10 Adhesive producers who have filed a DMF for HY-10 Adhesive include:

  - Adhesives Research Inc

Registrar Corp can help you to properly prepare and submit your HY-10 Adhesive DMF to FDA.

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

  - Format, assemble and deliver your HY-10 Adhesive DMF to FDA
  - Submit letters of authorization regarding your HY-10 Adhesive to FDA
 - Provide changes, additions and maintenance of your HY-10 Adhesive DMF
  - Respond to issues relating to ownership of your HY-10 Adhesive DMF
  - Assist with submission of responses to FDA concerning your HY-10 Adhesive DMF
  - Perform any required annual updates for your HY-10 Adhesive DMF

For more information about filing a DMF for HY-10 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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