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