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Track 3 Session 2: Clinical Evidence for Medical Devices
Session Chair(s)
Ashish Indani
Senior Manager – Clinical Affairs Neurovascular
Stryker Global Technology Center, India
Clinical Evidence for Medical Devices is regarded as one of the most revolutionary aspects of its entire lifecycle, involving numerous stakeholders. Unlike drugs, clinical evidence requirement for medical devices is not straightforward or systematic and is even discretional to some extent. In this session, the expertise of industry speakers will help you comprehend the optimal extent and method for Clinical Evidence of Medical Devices.
Speaker(s)
How Much And What Clinical Evidence Is Sufficient For Medical Devices?
Vinay Rajan
Medtronic India Pvt ltd, India
Senior Director
Dialogue: General Safety And Performance Requirements Vs. Essential Principles – What Should Be The Focus Of The CER?
Ashish Indani
Stryker Global Technology Center, India
Senior Manager – Clinical Affairs Neurovascular
Dialogue: General Safety And Performance Requirements Vs. Essential Principles – What Should Be The Focus Of The CER?
Ashokkumar Thakkar
Meril Life Sciences Pvt. Ltd., India
Head of Clinical Research
Contributing Panelist
Lipi Chakhaiyar
Abbott, India
Director Regulatory Affairs
Contributing Panelist
Gautam Wankhede
MyLab Discovery Solutions, India
Director Medical Affairs
Contributing Panelist
Rupam Chaudhary
Tata Consultancy Services Ltd., India
Global Head, Life Sciences Engineering
Contributing Panelist
Priyadarshini Arambam
General Manager - Clinical Research Operations, India
Academics & Research Department - Batra Hospital and Medical Research Centre
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