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Filing a DMF for DDU-310 Silicone Fluid with the U.S. FDA

Filing a drug master file (DMF) for DDU-310 Silicone Fluid can be a useful mechanism to market your DDU-310 Silicone Fluid to the U.S. Drug Industry. Typical DDU-310 Silicone Fluid producers who have filed a DMF for DDU-310 Silicone Fluid include:

  - Nusil Technology Llc

Registrar Corp can help you to properly prepare and submit your DDU-310 Silicone Fluid DMF to FDA.

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

  - Format, assemble and deliver your DDU-310 Silicone Fluid DMF to FDA
  - Submit letters of authorization regarding your DDU-310 Silicone Fluid to FDA
 - Provide changes, additions and maintenance of your DDU-310 Silicone Fluid DMF
  - Respond to issues relating to ownership of your DDU-310 Silicone Fluid DMF
  - Assist with submission of responses to FDA concerning your DDU-310 Silicone Fluid DMF
  - Perform any required annual updates for your DDU-310 Silicone Fluid DMF

For more information about filing a DMF for DDU-310 Silicone Fluid, 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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