##  [8000+ Successful Submissions in eCTD Format to Multiple Regions](/index%2ephp/case-studies/8000-successful-submissions-in-ectd-format-to-multiple-regions) 

- [Medicinal Products](/index%2ephp/case-studies-main-categories/medicinal-products)
- [Publishing and Submission](/index%2ephp/case-studies-main-categories/publishing-and-submission)





[Global](/index%2ephp/case-studies-heath-authority/global)

 

 ![8000+ Successful Submissions in eCTD Format to Multiple Regions]()

The client is a Germany based global leader in the pharmaceutical and healthcare industry. The company was planning to expand its operations in the US, EU, GCC and Canada regions. In order to do so, the client was looking for Regulatory assistance with the submission of detailed information in the eCTD format. The challenge faced by the client was decoding the regional requirement for every country.

Download the case study to comprehend how Freyr leveraged its Regulatory knowledge to file 8000+ submissions per annum, compliantly, within the given timeline.



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