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HomeDrugsDrug Master Files (DMF)DMF ExamplesType IV DMFs › U.S. FDA St-Cyclomethicone 5-NF Regulations

Filing a DMF for St-Cyclomethicone 5-NF with the U.S. FDA

Filing a drug master file (DMF) for St-Cyclomethicone 5-NF can be a useful mechanism to market your St-Cyclomethicone 5-NF to the U.S. Drug Industry. Typical St-Cyclomethicone 5-NF producers who have filed a DMF for St-Cyclomethicone 5-NF include:

  - Dow Corning Corp

Registrar Corp can help you to properly prepare and submit your St-Cyclomethicone 5-NF DMF to FDA.

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

  - Format, assemble and deliver your St-Cyclomethicone 5-NF DMF to FDA
  - Submit letters of authorization regarding your St-Cyclomethicone 5-NF to FDA
 - Provide changes, additions and maintenance of your St-Cyclomethicone 5-NF DMF
  - Respond to issues relating to ownership of your St-Cyclomethicone 5-NF DMF
  - Assist with submission of responses to FDA concerning your St-Cyclomethicone 5-NF DMF
  - Perform any required annual updates for your St-Cyclomethicone 5-NF DMF

For more information about filing a DMF for St-Cyclomethicone 5-NF, 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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