Medical Device & Diagnostics Summit

Join industry leaders and experts at Veeva Medical Device & Diagnostics Summit on June 1 – 2, 2020 in Minneapolis to learn how organizations are shortening the product development lifecycle and keeping pace with evolving regulations such as MDR.

Meet your medical device community to exchange best practices and share how innovation streamlines content and data management in commercial, clinical, quality, and regulatory.

Key themes include improving transparency and collaboration between internal and external stakeholders to cuts costs, maintain compliance, and deliver higher quality and more effective therapies to patients.

Veeva Medical Device & Diagnostics Summit is complimentary to Veeva customers and invited guests. Space is limited.

Register

Key topics will include:

Commercial Content
Combine digital asset management with review and distribution capabilities for end-to-end compliance.
Clinical Trial Management
Streamline end-to-end clinical trial processes with unified applications for clinical operations and clinical data management to improve study visibility and performance.
Quality Management
Bring together quality processes and content to improve compliance and operational innovation.
Regulatory Information Management
Keep pace with changing regulations and growing complexity in product development.

Top 5 Reasons You Should Attend

Become an active member of the Veeva Medical Device & Diagnostics community
Move the industry forward.
Maximize your Veeva investments
Discover best practices to get the most out of your Veeva solutions.
Gain perspective from the greatest medical device minds
Hear from innovative medical device companies and Veeva experts.
Get a front row seat to Veeva news
Be the first to know about new Veeva innovations, announcements, and feature updates.
Interact and have fun
Network with your peers and develop new industry partnerships.