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Filing a DMF for BD Readyfill with the U.S. FDA

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

  - Becton Dickinson and Co

Registrar Corp can help you to properly prepare and submit your BD Readyfill DMF to FDA.

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

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

For more information about filing a DMF for BD Readyfill, 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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