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Filing a DMF for Lauroglycol with the U.S. FDA

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

  - Gatefosse Sa

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

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

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

For more information about filing a DMF for Lauroglycol, 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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