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