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Filing a DMF for MS-H-Medshield 1008 with the U.S. FDA

Filing a drug master file (DMF) for MS-H-Medshield 1008 can be a useful mechanism to market your MS-H-Medshield 1008 to the U.S. Drug Industry. Typical MS-H-Medshield 1008 producers who have filed a DMF for MS-H-Medshield 1008 include:

  - Berry Plastics Corp Tapes & Coatings Division

Registrar Corp can help you to properly prepare and submit your MS-H-Medshield 1008 DMF to FDA.

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

  - Format, assemble and deliver your MS-H-Medshield 1008 DMF to FDA
  - Submit letters of authorization regarding your MS-H-Medshield 1008 to FDA
 - Provide changes, additions and maintenance of your MS-H-Medshield 1008 DMF
  - Respond to issues relating to ownership of your MS-H-Medshield 1008 DMF
  - Assist with submission of responses to FDA concerning your MS-H-Medshield 1008 DMF
  - Perform any required annual updates for your MS-H-Medshield 1008 DMF

For more information about filing a DMF for MS-H-Medshield 1008, 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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