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Live Webinar with Q&A

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Today, medtech clinical trials need to be conducted faster and more efficiently, while maintaining accuracy and data integrity. Learn how you can speed trials by unifying clinical systems and processes on a single cloud platform.
Veeva strategy and product experts will share how the end-to-end Clinical Platform unifies operations and data management to streamline trials from start to finish, including:
A comprehensive demo highlighting EDC, CTMS, and eTMF
An overview of the dashboards you can access within EDC
Auto-filling capabilities within eTMF
How to plan and document monitoring visits
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00:00 am – 00:00 am PT |
Connect |
00:00 am – 00:00 am PT |
Zone Specific Sessions |
00:00 am – 00:00 am PT |
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00:00 am – 00:00 am PT |
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Senior Director, Clinical Strategy
Veeva
With more than 20 years of experience in data management, clinical research, project management, and product management, John is focused on optimizing processes to enable compliant, end-to-end clinical trial execution and evidence generation. He holds an MBA and MPH, and has served in leadership roles in medtech and biopharma companies prior to joining Veeva MedTech.

Senior Manager, Solution Consulting, Clinical Data
Veeva
Eric has over 25 years of pharmaceutical and medical device industry experience. The majority of this time has been focused on data management and technology adoption. Today, he leads Veeva’s team of Solution Consultants for Clinical Data products.


















Demo
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