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