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Track 3 Session 2: Clinical Evidence for Medical Devices
Session Chair(s)
Ashish Indani
Managing Director, Krishnamugdha Advance ResearchTeck, 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?
Medical/Clinical Affairs, Training & Education Leader - APAC, Medtronic, India
Dialogue: General Safety And Performance Requirements Vs. Essential Principles – What Should Be The Focus Of The CER?
Healthcare Industry Leader, India
With Additional Participation Of:
CEO and Medical Device Regulatory Advisor, Symbiorph Clinical Trialogy, India
Contributing Panelist
Head of Clinical Research, Meril Life Sciences Pvt. Ltd., India
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