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Filing a DMF for MS-H-2530SR with the U.S. FDA

Filing a drug master file (DMF) for MS-H-2530SR can be a useful mechanism to market your MS-H-2530SR to the U.S. Drug Industry. Typical MS-H-2530SR producers who have filed a DMF for MS-H-2530SR include:

  - Berry Plastics Corp Tapes & Coatings Division

Registrar Corp can help you to properly prepare and submit your MS-H-2530SR DMF to FDA.

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

  - Format, assemble and deliver your MS-H-2530SR DMF to FDA
  - Submit letters of authorization regarding your MS-H-2530SR to FDA
 - Provide changes, additions and maintenance of your MS-H-2530SR DMF
  - Respond to issues relating to ownership of your MS-H-2530SR DMF
  - Assist with submission of responses to FDA concerning your MS-H-2530SR DMF
  - Perform any required annual updates for your MS-H-2530SR DMF

For more information about filing a DMF for MS-H-2530SR, 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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