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.


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.

Meet great people, learn new things

You will be among industry professionals who are equally passionate about innovation and improving the product development lifecycle. Summit provides a number of ways to expand your network, learn, and share including:

Welcome Reception: Exchange ideas, share expertise, and have some fun!
Deep-dive Sessions: Hear from leaders and product experts to discuss industry opportunities including commercial, clinical operations, clinical data management, quality, and regulatory.
Networking Lunch: Participate in customer-led discussions while enjoying lunch.