Home · Events · R&D Summit · North America

September 16-18, Philadelphia, PA

“I came home brimming with ideas for best practice implementation
and was impressed by the level of attention paid by the Veeva
Leadership team. I had the opportunity to engage with all
leaders in a very constructive way.”

Karen Whonder | Manager, Clinical Operations Systems at Macrogenics

“I appreciate that Veeva’s leadership is making themselves
available to clients so we can have open conversations. The consensus
was unanimous – all of your SMB clients want to implement more Veeva.”

Amy Benton | Sr. Director, IT at Retrophin

“Great Executive Roundtable with excellent presentations
from Ken Getz leading the discussion.”

Dawn M. Furey | Executive Director, Head of Global Operations,
Global Clinical Trial Operations at Merck & Co.

2018 Veeva R&D Summit, North America

2018 Veeva R&D Summit registration is now open – reserve your spot today!

Veeva R&D Summit is an annual gathering of pharma, biotech, and medical device and diagnostics leaders in clinical, regulatory, quality, and IT. Join more than 1,300 life sciences leaders and experts to share best practices and see what’s coming next in the industry.

R&D Summit will be held at the Pennsylvania Convention Center. The event begins with a welcome reception on Sunday, September 16 from 6:00 p.m. – 8:00 p.m. and ends with user community meetings throughout the afternoon of Tuesday, September 18.

Last year we heard case studies from Eli Lilly, Ora, Inc., Daiichi Sankyo, C.R. Bard, UCB, REGENXBIO, and many more. This year’s key topics include:

Clinical Operations

Transforming end-to-end clinical trial processes with a unified clinical suite.

Enhancing collaboration and data sharing between sponsors, CROs, and investigator sites.

Supporting trial efficiency, quality, and completeness.

Enabling active TMF operating models within a unified clinical environment.

Clinical Data

Speeding study timelines, including study build and database lock.

Collecting and managing complete and concurrent data.

Streamlining end-to-end processes with EDC- CTMS integration.

Enabling sites for success with faster data entry.

Regulatory

Automating submission development from planning through publishing.

Managing product variations and tracking approval status.

Aligning headquarters and affiliates to optimize regulatory processes.

Eliminating spreadsheets for health authority interactions.

Quality and Manufacturing

Building a high performance quality organization with real-time visibility.

Driving inspection-readiness with unified training.

Quality management learnings and deployment best practices.

Modernizing change management.

Veeva Vault Platform (NEW)

Extending Vault with Vault Objects and SDK.

Data management strategy across Vaults.

Vault security best practices.

Gaining insight with reporting and dashboards.

Who Should Attend

This two-day event is dedicated to R&D professionals in the life sciences industry. You will benefit from attending R&D Summit if you are primarily focused on clinical operations, clinical data management, regulatory, quality and manufacturing, or IT.

Register now for an exclusive look at the latest innovations and capabilities coming your way. This is a complimentary event for Veeva customers and select invited guests.

Previous Attendees

Here is a snapshot of companies who attended last year’s conference.

Bringing the Industry’s Leaders Together

Leaders in clinical operations, clinical data management, regulatory, and quality and manufacturing will have the opportunity to come together and discuss solutions for some of the industry’s toughest challenges during leadership roundtable discussions on Day 1 of 2018 R&D Summit. Attendance for leadership roundtable discussions is by invitation only.