##  [Filing of various meeting requests for IND, NDA, and ANDA](/case-studies/filing-of-various-meeting-requests-for-ind-nda-and-anda) 

- [Medicinal Products](/case-studies-main-categories/medicinal-products)
- [Publishing and Submission](/case-studies-main-categories/publishing-and-submission)





[US FDA](/case-studies-heath-authority/us-fda)

 

 ![Filing of various meeting requests for IND, NDA, and ANDA]()

A USA-based innovative pharmaceutical company approached Freyr for Regulatory support in filing pre-IND (Type B) meeting requests, type C meeting briefing materials, and promotional labeling advertising with the US FDA. Freyr analyzed the client’s existing processes to identify some of the significant constraints, such as tracking versions of frequently changed documents and replacing the same in eCTD, taking care of end-to-end publishing activities from study documents to final Electronic Submission Gateway (ESG) submission.

Discover how Freyr provided a valid submission to the Agency with zero errors and warnings by dedicating full-time resources with continuous support. Download the proven case.



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