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