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Reducing Pharma Regulatory Submission Turnaround Time by 20%

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The client is a top-10 global pharmaceutical company. They wanted to quickly register their existing products in new markets such as Europe, Canada, and the U.S. They needed a scalable and flexible operating model along with a team with expertise in global regulatory requirements. They chose Syntel as their partner, based on our expertise and ability to meet their stringent deadlines.

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http://www.syntelinc.com/sites/default/files/success_stories_pdf/SYNT_Life_Sciences_Regulatory_Case_Study.pdf

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