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