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Filing a DMF for EQ-Pak Sachet with the U.S. FDA

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

  - Airsec Sa

Registrar Corp can help you to properly prepare and submit your EQ-Pak Sachet DMF to FDA.

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

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

For more information about filing a DMF for EQ-Pak Sachet, 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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