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Filing a DMF for MS-H-HBFW-48 with the U.S. FDA

Filing a drug master file (DMF) for MS-H-HBFW-48 can be a useful mechanism to market your MS-H-HBFW-48 to the U.S. Drug Industry. Typical MS-H-HBFW-48 producers who have filed a DMF for MS-H-HBFW-48 include:

  - Berry Plastics Corp Tapes & Coatings Division

Registrar Corp can help you to properly prepare and submit your MS-H-HBFW-48 DMF to FDA.

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

  - Format, assemble and deliver your MS-H-HBFW-48 DMF to FDA
  - Submit letters of authorization regarding your MS-H-HBFW-48 to FDA
 - Provide changes, additions and maintenance of your MS-H-HBFW-48 DMF
  - Respond to issues relating to ownership of your MS-H-HBFW-48 DMF
  - Assist with submission of responses to FDA concerning your MS-H-HBFW-48 DMF
  - Perform any required annual updates for your MS-H-HBFW-48 DMF

For more information about filing a DMF for MS-H-HBFW-48, 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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