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

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

  - Dow Chemical Co Michigan Div

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

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

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

For more information about filing a DMF for Methocel, 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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