428 Veeva Systems Testimonials

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

"Now our customers can do insight-driven, multichannel selling across both existing and future channels."

"A solid data foundation, specifically a single source of customer data, is essential to meet our omnichannel aspirations."

"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."

"A RIM system starts to become a strategic asset for organizations that do it right."

"Approved Notes allows our reps to capture detailed notes, insights, and next steps directly into the account record in Veeva CRM. Free-text monitoring combs through post-call notes for words and phrases that we find egregious so we can address the issue."

"The implementation is the beginning of the conversation with your customers, it’s not the end."

“The clinical trial industry must constantly embrace change to stay competitive and the emergence of COVID-19 is increasing the rate of this necessary change faster than anyone could anticipate.”

"To make a mark in the clinical research space, you've got to do it better, smarter, and faster than everybody else."

“Frankly, I get excited by the business insights that come with free text. I think it’s bringing insights to the business in some kind of real-time fashion so business leaders can take action on trends, whether that’s business trends or compliance risk."

"This vision of unified quality is appealing. All processes are in one system, which allows for automation to be baked into the standard product."

“Incredibly rapid, 12 week deployment of Vault Safety.”

“Veeva Summits bring the industry together in an authentic, engaging, and stimulating way. I'm looking forward to being part of this year's dedicated Medical Device & Diagnostics Summit, because it will be a unique opportunity to bring this passionate community together and share ideas on how to improve overall Dx study management in Veeva.”

“With a continuous model, regulatory teams can identify any errors and address broken links to source data as the submission is being built so teams don’t have to go through the lengthy re-publishing process over and over. Using this system, we have cut submission time by at least half.”

"When I calculate the amount of manual time it takes to receive a regulatory document and process it to the point of being monitored and filed away, I estimate we save at least 50% of time per document using Veeva SiteVault.”