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Filing a DMF for 38mm Closure with the U.S. FDA

Filing a drug master file (DMF) for 38mm Closure can be a useful mechanism to market your 38mm Closure to the U.S. Drug Industry. Typical 38mm Closure producers who have filed a DMF for 38mm Closure include:

  - Plaspak Closures Pty Ltd

Registrar Corp can help you to properly prepare and submit your 38mm Closure DMF to FDA.

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

  - Format, assemble and deliver your 38mm Closure DMF to FDA
  - Submit letters of authorization regarding your 38mm Closure to FDA
 - Provide changes, additions and maintenance of your 38mm Closure DMF
  - Respond to issues relating to ownership of your 38mm Closure DMF
  - Assist with submission of responses to FDA concerning your 38mm Closure DMF
  - Perform any required annual updates for your 38mm Closure DMF

For more information about filing a DMF for 38mm Closure, 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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