Latest version offers a streamlined site-centric experience to simplify relationships with study sponsors.
Veeva Systems has announced the newest release of Veeva Site Connect. New capabilities of the solution are headlined by a streamlined site-centric experience that will simplify and standardize site-sponsor relationships.1
The solution offers sponsors and sites a single place to collaborate, automating information flow throughout the lifecycle of a clinical trial. Information flow includes protocols, safety reports, payment letters, and more.
New features of Veeva Site Connect include:
“By standardizing how information is shared across all sites in one application with Veeva Site Connect, we aim to save time and effort that can be focused on treating patients,” a clinical operations excellence leader at a top 20 biopharma said in a press release. “Our goal is to eliminate manual handoffs and inefficiencies for faster site start-up, more efficient monitoring, and simplified study closeout.”
Veeva Site Connect is part of Veeva Clinical Platform, which is the provider’s complete solution for patients, sites, and sponsors. According to Veeva, seven of the top 20 biopharmas have already adopted Site Connect.
“I would be ecstatic if all our sponsors use Veeva Site Connect. It gives sites a much more efficient way to collaborate with sponsors, maintain regulatory compliance, and get critical therapies to patients faster,” Alisha Garibaldi, CEO, Skylight Health Research, said in the press release. “The less time we spend doing administrative work in systems, the more time we have to execute trials and help patients.”
Marta Jureczko-Hinzmann, head of global clinical solution services at AstraZeneca added, “By implementing Veeva Site Connect for our safety letter distribution process, we anticipate achieving a significant reduction in manual processing while enhancing oversight and compliance. Sharing safety letters across all sites globally within a single application will allow us to harmonize the entire process across the company and optimize how we allocate valuable resources.”
This announcement from Veeva comes just days before its R&D Quality Summit which will be taking place in Boston, MA, September 9-10.
1. Major Release of Veeva Site Connect Streamlines Clinical Trial Execution for Sites and Sponsors. News release. Veeva Systems. September 5, 2024. Accessed September 5, 2024. https://www.veeva.com/resources/major-release-of-veeva-site-connect-streamlines-clinical-trial-execution-for-sites-and-sponsors/
Stay current in clinical research with Applied Clinical Trials, providing expert insights, regulatory updates, and practical strategies for successful clinical trial design and execution.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Managing Side Effects and Dosing in Off-Label GLP-1 Use with Help from Real-World Evidence
July 18th 2025Shipra Patel, global therapeutic area section head, endocrinology, global head, pediatrics, Parexel, explains how real-world data is helping researchers navigate gastrointestinal side effects, dose flexibility, and long-term tolerability in off-label GLP-1 use.
Anselamimab Misses Primary Endpoint in Phase III CARES Trials for AL Amyloidosis
July 17th 2025In the Phase III CARES trials, anselamimab did not meet the primary endpoint for advanced-stage AL amyloidosis, but a prespecified subgroup analysis revealed meaningful improvements in survival and cardiovascular outcomes.