戻る Agenda
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?
Debashis Das
Medtronic, India
Medical/Clinical Affairs, Training & Education Leader - APAC
Dialogue: General Safety And Performance Requirements Vs. Essential Principles – What Should Be The Focus Of The CER?
Srirupa Das
Johnson & Johnson Private Limited, India
Country Medical Director
With Additional Participation Of:
Siddharth Jain
Symbiorph Clinical Trialogy, India
CEO and Medical Device Regulatory Advisor
Contributing Panelist
Ashokkumar Thakkar
Meril Life Sciences Pvt. Ltd., India
Head of Clinical Research