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