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HomeDrugsDrug Master Files (DMF)DMF ExamplesType IV DMFs › U.S. FDA Roderm MD-153 Rubber Adhesive Regulations

Filing a DMF for Roderm MD-153 Rubber Adhesive with the U.S. FDA

Filing a drug master file (DMF) for Roderm MD-153 Rubber Adhesive can be a useful mechanism to market your Roderm MD-153 Rubber Adhesive to the U.S. Drug Industry. Typical Roderm MD-153 Rubber Adhesive producers who have filed a DMF for Roderm MD-153 Rubber Adhesive include:

  - Rohm and Haas Co

Registrar Corp can help you to properly prepare and submit your Roderm MD-153 Rubber Adhesive DMF to FDA.

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

  - Format, assemble and deliver your Roderm MD-153 Rubber Adhesive DMF to FDA
  - Submit letters of authorization regarding your Roderm MD-153 Rubber Adhesive to FDA
 - Provide changes, additions and maintenance of your Roderm MD-153 Rubber Adhesive DMF
  - Respond to issues relating to ownership of your Roderm MD-153 Rubber Adhesive DMF
  - Assist with submission of responses to FDA concerning your Roderm MD-153 Rubber Adhesive DMF
  - Perform any required annual updates for your Roderm MD-153 Rubber Adhesive DMF

For more information about filing a DMF for Roderm MD-153 Rubber Adhesive, 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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