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HomeDrugsDrug Master Files (DMF)DMF ExamplesType IV DMFs › U.S. FDA Chlorofluorocarbon 11, 12, and 114 Regulations

Filing a DMF for Chlorofluorocarbon 11, 12, and 114 with the U.S. FDA

Filing a drug master file (DMF) for Chlorofluorocarbon 11, 12, and 114 can be a useful mechanism to market your Chlorofluorocarbon 11, 12, and 114 to the U.S. Drug Industry. Typical Chlorofluorocarbon 11, 12, and 114 producers who have filed a DMF for Chlorofluorocarbon 11, 12, and 114 include:

  - CFC Consortium

Registrar Corp can help you to properly prepare and submit your Chlorofluorocarbon 11, 12, and 114 DMF to FDA.

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

  - Format, assemble and deliver your Chlorofluorocarbon 11, 12, and 114 DMF to FDA
  - Submit letters of authorization regarding your Chlorofluorocarbon 11, 12, and 114 to FDA
 - Provide changes, additions and maintenance of your Chlorofluorocarbon 11, 12, and 114 DMF
  - Respond to issues relating to ownership of your Chlorofluorocarbon 11, 12, and 114 DMF
  - Assist with submission of responses to FDA concerning your Chlorofluorocarbon 11, 12, and 114 DMF
  - Perform any required annual updates for your Chlorofluorocarbon 11, 12, and 114 DMF

For more information about filing a DMF for Chlorofluorocarbon 11, 12, and 114, 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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