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

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

  - Promens Sa

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

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

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

For more information about filing a DMF for Easylock, 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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