##  [345, 177 and 198 Successful Submissions for ROW, Europe and the USA Respectively Within 3 Months](/index%2ephp/case-studies/345-177-and-198-successful-submissions-for-row-europe-and-the-usa-respectively-within-3-months) 

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





[EMA](/index%2ephp/case-studies-heath-authority/ema)

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

[US FDA](/index%2ephp/case-studies-heath-authority/us-fda)

 

 ![345, 177 and 198 Successful Submissions for ROW, Europe and the USA Respectively Within 3 Months]()

A Switzerland-based global, Pharma company approached Freyr for life cycle management publishing for their pharma and consumer healthcare products. As the project needs submissions for various authorities in the RoW, Europe and the USA markets within very short timelines, analyzing and executing the Regulatory activity was initially challenging for Freyr.

Read this case study to decode how Freyr overcame the procedural hurdles for publishing and submission in a very short time and dispatched significant amount of submissions for each region.



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