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