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