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Filing a DMF for Noryl (R) Thermoplastic with the U.S. FDA

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

  - General Electric Company

Registrar Corp can help you to properly prepare and submit your Noryl (R) Thermoplastic DMF to FDA.

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

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

For more information about filing a DMF for Noryl (R) Thermoplastic, 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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