Sourav Gupta's Blog

Sourav Gupta has 14+ years of experience supporting the Life Sciences industry in the clinical,...


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Posted on: March 26-2018 | By : Sourav Gupta | In: Industries,Life Sciences | No Comments
The journey so far   Year 2017 was a learning phase for the Medical Device industry. With the official launch of the European Medical Device Regulations (EU MDR 2017/745) and European In-Vitro Diagnostic Regulations (EU IVDR 2017/746), many medical device and in-vitro diagnostic companies faced uncertainty and confusion over the new requirements, as well as risks and challenges to their business.
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