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Filing a DMF for Plastic Injection Molded Closures with the U.S. FDA

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

  - Tri State Distribution

Registrar Corp can help you to properly prepare and submit your Plastic Injection Molded Closures DMF to FDA.

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

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

For more information about filing a DMF for Plastic Injection Molded Closures, 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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