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Filing a DMF for Empty Gelatin Capsule with the U.S. FDA

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

  - Shing Lih Fang Enterprise Co Ltd

Registrar Corp can help you to properly prepare and submit your Empty Gelatin Capsule DMF to FDA.

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

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

For more information about filing a DMF for Empty Gelatin Capsule, 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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