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Filing a DMF for Compressed Gas Cylinder Package with the U.S. FDA

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

  - Luxfer Gas Cylinders

Registrar Corp can help you to properly prepare and submit your Compressed Gas Cylinder Package DMF to FDA.

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

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

For more information about filing a DMF for Compressed Gas Cylinder Package, 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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