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Filing a DMF for Lexan R Polycarbonate Resins with the U.S. FDA

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

  - General Electric Company

Registrar Corp can help you to properly prepare and submit your Lexan R Polycarbonate Resins DMF to FDA.

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

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

For more information about filing a DMF for Lexan R Polycarbonate Resins, 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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