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의약품Drug Master Files (DMF)DMF ExamplesType III DMFs › U.S. FDA Adcote 548E and Coreactant F Regulations

Filing a DMF for Adcote 548E and Coreactant F with the U.S. FDA

Filing a drug master file (DMF) for Adcote 548E and Coreactant F can be a useful mechanism to market your Adcote 548E and Coreactant F to the U.S. Drug Industry. Typical Adcote 548E and Coreactant F producers who have filed a DMF for Adcote 548E and Coreactant F include:

  - Rohm and Haas Co

Registrar Corp can help you to properly prepare and submit your Adcote 548E and Coreactant F DMF to FDA.

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

  - Format, assemble and deliver your Adcote 548E and Coreactant F DMF to FDA
  - Submit letters of authorization regarding your Adcote 548E and Coreactant F to FDA
 - Provide changes, additions and maintenance of your Adcote 548E and Coreactant F DMF
  - Respond to issues relating to ownership of your Adcote 548E and Coreactant F DMF
  - Assist with submission of responses to FDA concerning your Adcote 548E and Coreactant F DMF
  - Perform any required annual updates for your Adcote 548E and Coreactant F DMF

For more information about filing a DMF for Adcote 548E and Coreactant F, simply click below:




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U.S. FDA Regulations:

U.S. FDA DMF Regulation: 21 C.F.R. Section 314.420


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