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