428 Veeva Systems Testimonials

“Before, we used 35 Excel workbooks to track submissions and correspondence. We now use Vault RIM and have comprehensive visibility across regulatory activities and information.”

“The Veeva tool is excellent. To have our customer interaction objectives aligned to our team’s strategic objectives gives users insight into what matters most to leadership and we can see it via the real-time dashboard in the same fashion as our managers. Veeva is the fi rst big step to incorporating strategic objectives that are most important to our customers and our organization into day-to-day planning.”

“Veeva is helping us transform our entire R&D business.”

"[Veeva CRM] allows our sales team to target their approach more effectively and provide better support to physicians.”

"Jennifer’s role includes executive oversight of product development, testing, clinical studies, medical/scientific writing, and regulatory submissions for medical devices. She is Cook’s Global Leader for Clinical Affairs which is responsible for the design, oversight, and management of pre-market and post-market clinical projects. She also collaborates with experts on Good Clinical Practice (GCP) including the international standard ISO 14155 (Clinical standard for conducting medical device studies)."

"We needed a system with the flexibility to adapt to the growth that was coming."

"Our goals were to achieve better quality outcomes by improving efficiency, oversight, and decision making."

"The biggest advantage is that we capture all surgeon interactions and the specific insights we get from the field. To have all of that in one place, visible to the entire team, is very valuable."

"The connection between medical inquiry records and scientific information was the turning point for medical affairs. Medical inquiry records are now the backbone of our system."

"Veeva Nitro is fast and easy. It works globally, regionally, and locally. It integrates extremely well with Veeva’s other products and does not require extensive configuration. That gave us a competitive advantage during lockdown because we really understood what was happening."

"The builds were fast and effective. We’ve had CROs with other systems take 10-12 weeks for each study build, even when the studies use the same system, the same page, and the same format. But the Veeva team made all the updates based on the original protocol in just six weeks. Veeva has been building the database for all our studies over the past three years and the average build time is at least 50% faster than before."

"This solution [between Vault EDC and Suvoda IRT] created simplicity at every level and for all stakeholders, the site, data management, the operational team, and for the drug supply team."

"I can’t imagine using two systems for MLR review and DAM — one solution for both is incomparable."

"Thinking about this as a technology project is not correct. You really have to help people transform the way they work."

"Nearly 30 years’ experience in clinical trials and statistical sciences across all phases of product development in industry, academia, and NIH settings. Currently leads Alcon’s Clinical R&D team responsible for the strategic and operational design, execution, and reporting of all Alcon clinical development activities and all global medical affairs brand plans for Alcon’s pipeline and existing marketed portfolio of products."