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Filing a DMF for Laminate Collapsible Tubing with the U.S. FDA

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

  - Neopac Ag

Registrar Corp can help you to properly prepare and submit your Laminate Collapsible Tubing DMF to FDA.

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

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

For more information about filing a DMF for Laminate Collapsible Tubing, 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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