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

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

  - Solvay Fluor Und Derivate Gmbh

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

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

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

For more information about filing a DMF for Norflurane, 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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