Filing a drug master file (DMF) for MA-73B can be a useful mechanism to market your
MA-73B to the U.S. Drug Industry. Typical MA-73B producers who have filed a DMF for
Adhesives Research Inc
Registrar Corp can help you to properly prepare and submit your MA-73B DMF to FDA.
As your Agent, Registrar Corp will perform the following administrative functions:
Format, assemble and deliver your MA-73B DMF to FDA
Submit letters of authorization regarding your MA-73B to FDA
Provide changes, additions and maintenance of your MA-73B DMF
Respond to issues relating to ownership of your MA-73B DMF
Assist with submission of responses to FDA concerning your MA-73B DMF
Perform any required annual updates for your MA-73B DMF
For more information about filing a DMF for MA-73B, 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.