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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Sourav Gupta

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

 
Posted on: March 12-2018 | By : Imran Sheikh | In: Life Sciences | 1 Comment
Although high-profile data breaches grab the headlines, behind the scenes, life sciences is just as information sensitive as any industry. Any pharma company faces a major challenge when it comes to complying with the myriad regulatory requirements about how they create, handle and submit documentation about the products they manufacture.

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Imran Sheikh

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Imran Sheikh
Imran Sheikh is Sr. Consultant, Regulatory Affairs at Syntel. He has over 10 years of rich...

 
 

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