Filing a drug master file (DMF) for MPEG5000 can be a useful mechanism to market your
MPEG5000 to the U.S. Drug Industry. Typical MPEG5000 producers who have filed a DMF for
Shearwater Polymers Inc
Registrar Corp can help you to properly prepare and submit your MPEG5000 DMF to FDA.
As your Agent, Registrar Corp will perform the following administrative functions:
Format, assemble and deliver your MPEG5000 DMF to FDA
Submit letters of authorization regarding your MPEG5000 to FDA
Provide changes, additions and maintenance of your MPEG5000 DMF
Respond to issues relating to ownership of your MPEG5000 DMF
Assist with submission of responses to FDA concerning your MPEG5000 DMF
Perform any required annual updates for your MPEG5000 DMF
For more information about filing a DMF for MPEG5000, simply click below:
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.