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Filing a DMF for Metered Dose Valves with the U.S. FDA

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

  - Valois Sas

Registrar Corp can help you to properly prepare and submit your Metered Dose Valves DMF to FDA.

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

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

For more information about filing a DMF for Metered Dose Valves, 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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