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HomeDrugsDrug Master Files (DMF)DMF ExamplesType IV DMFs › U.S. FDA Dow Corning 360 Medical Grade Fluid Regulations

Filing a DMF for Dow Corning 360 Medical Grade Fluid with the U.S. FDA

Filing a drug master file (DMF) for Dow Corning 360 Medical Grade Fluid can be a useful mechanism to market your Dow Corning 360 Medical Grade Fluid to the U.S. Drug Industry. Typical Dow Corning 360 Medical Grade Fluid producers who have filed a DMF for Dow Corning 360 Medical Grade Fluid include:

  - Dow Corning Corp

Registrar Corp can help you to properly prepare and submit your Dow Corning 360 Medical Grade Fluid DMF to FDA.

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

  - Format, assemble and deliver your Dow Corning 360 Medical Grade Fluid DMF to FDA
  - Submit letters of authorization regarding your Dow Corning 360 Medical Grade Fluid to FDA
 - Provide changes, additions and maintenance of your Dow Corning 360 Medical Grade Fluid DMF
  - Respond to issues relating to ownership of your Dow Corning 360 Medical Grade Fluid DMF
  - Assist with submission of responses to FDA concerning your Dow Corning 360 Medical Grade Fluid DMF
  - Perform any required annual updates for your Dow Corning 360 Medical Grade Fluid DMF

For more information about filing a DMF for Dow Corning 360 Medical Grade Fluid, 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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