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The impact of the GDPR on Medical Device Clinical Investigations
Gadi Ginot, CEO and Founder, Physio-Logic

  13rd, June 2018
Wed, 15:30 – 16:00

NOTE: We do NOT plan to send a replay, so mark your calander

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Join us for a 20 minute overview of the GDPR regulation and its impact on medical device clinical trials.

The presentation will be followed by a 10 minutes Q&A session.

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Gadi Ginot
Gadi GinotCEO & Founder, Physio-Logic

Gadi Ginot is the founder of Physio-Logic Ltd, Israel’s largest and leading provider of accelerated medical device approval, certification and regulatory compliance solutions.

He is internationally renowned for his leadership in medical device regulations. What sets Gadi apart from other regulatory professionals is his multi-disciplinary education in science, business and medicine, knowhow and hands-on experience mastering both medical device regulation, quality assurance and clinical trials. This synergy powers the innovative regulatory strategies that paved the path to market in the USA, the EU and the Far East of many innovative device within unprecedented time lines boosting return on investment (ROI).

Gadi brings forward over 23 years’ experience in the biotech industry, from entry to the VP level, residing in three continents (EU, US, Israel), serving global corporate as well as start-ups. His track record include over 50 expedited device approvals, at record times, negotiating successfully the US FDA, Notified Bodies and Israeli MOH to accept out of the box regulatory and clinical strategies. Gadi is a sought-after lecturer and mentor in numerous prestigious academic programs, accelerators and hubs.

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Please note that this webinar is intended for medical device manufacturers only. The organizers reserve the right for changes and to deny registration requests. Please confirm (required)