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Filing a DMF for Bag-On-Valve with the U.S. FDA

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

  - EP Spray Systems

Registrar Corp can help you to properly prepare and submit your Bag-On-Valve DMF to FDA.

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

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

For more information about filing a DMF for Bag-On-Valve, 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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