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Filing a DMF for Cremophor Surfactant RH40 with the U.S. FDA

Filing a drug master file (DMF) for Cremophor Surfactant RH40 can be a useful mechanism to market your Cremophor Surfactant RH40 to the U.S. Drug Industry. Typical Cremophor Surfactant RH40 producers who have filed a DMF for Cremophor Surfactant RH40 include:

  - BASF SE

Registrar Corp can help you to properly prepare and submit your Cremophor Surfactant RH40 DMF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Format, assemble and deliver your Cremophor Surfactant RH40 DMF to FDA
  - Submit letters of authorization regarding your Cremophor Surfactant RH40 to FDA
 - Provide changes, additions and maintenance of your Cremophor Surfactant RH40 DMF
  - Respond to issues relating to ownership of your Cremophor Surfactant RH40 DMF
  - Assist with submission of responses to FDA concerning your Cremophor Surfactant RH40 DMF
  - Perform any required annual updates for your Cremophor Surfactant RH40 DMF

For more information about filing a DMF for Cremophor Surfactant RH40, simply click below:




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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.
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