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