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Filing a DMF for Infuking 200 with the U.S. FDA

Filing a drug master file (DMF) for Infuking 200 can be a useful mechanism to market your Infuking 200 to the U.S. Drug Industry. Typical Infuking 200 producers who have filed a DMF for Infuking 200 include:

  - Wihuri Oy

Registrar Corp can help you to properly prepare and submit your Infuking 200 DMF to FDA.

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

  - Format, assemble and deliver your Infuking 200 DMF to FDA
  - Submit letters of authorization regarding your Infuking 200 to FDA
 - Provide changes, additions and maintenance of your Infuking 200 DMF
  - Respond to issues relating to ownership of your Infuking 200 DMF
  - Assist with submission of responses to FDA concerning your Infuking 200 DMF
  - Perform any required annual updates for your Infuking 200 DMF

For more information about filing a DMF for Infuking 200, 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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