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Filing a DMF for Triethyl Citrate FCC with the U.S. FDA

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

  - Vertellus Performance Materials Inc

Registrar Corp can help you to properly prepare and submit your Triethyl Citrate FCC DMF to FDA.

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

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

For more information about filing a DMF for Triethyl Citrate FCC, 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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