Veeva Systems’ Post

Watch the interview with Frank Armenante 👉 https://lnkd.in/gvdwG2bj

Continuous publishing streamlines and accelerates the submission process from planning to publishing and fosters a seamless adaptation to industry changes like eCTD 4.0 and IDMP. Learn more https://bit.ly/3RPgewG Regulatory Affairs Professionals Society (RAPS) #regulatoryoperations #submissionpublishing #pharmaceuticals

pharmaphorum sits down with Chris Moore at the 10th #VeevaSummitEU to discuss ways connected technology is reducing friction across the R&D lifecycle for better operational and patient outcomes. Watch the video in pharmaphorum: https://lnkd.in/emUx6bBv #lifesciences #pharmaceuticals

Why do over 2,000 R&D and quality leaders and experts attend #VeevaSummit every year? To move the industry forward through information sharing, joint problem-solving, and building new connections. See for yourself what Summit is all about this September 9-10 in Boston: https://bit.ly/3xZFXvp #pharmaceuticals #biotechnology

“.. the most innovative technology and a flexible partner, both of which Veeva delivered on.” Frank Armenante shares his thoughts on Novo Nordisk’s decision to commit to Vault CRM. #biopharma #pharmaceuticals #lifesciences

Veeva’s #AI Partner Program adds five new members: Anthill Agency, Hyntelo, ODAIA, Translations.com, and ZS! These companies are bringing advanced technology and support to integrate GenAI seamlessly to Veeva Vault applications. Learn more: https://lnkd.in/eQzKRicZ #lifesciences #pharmaceuticals

Dan Rizzo sits down with Pharmaceutical Executive to share the latest #VeevaPulse findings on the status of HCP access and what new models field teams are using to break through. https://lnkd.in/gdW9ycWG #hcpaccess #pharmaceuticals #lifesciences

Cell and gene therapies are taking the industry by storm, but paper systems for quality control hold up timelines. Mike Edwards spoke with Clinical Trials Arena at #VeevaSummitEU to discuss how to speed up the process. https://lnkd.in/dZW8cPGj #lifesciences #manufacturing #pharmaceuticals

Changing to a new EDC provider can feel daunting while staying productive with normal work. Access this free, how-to guide which details 5 key tips for simplifying the change management process and ensuring a successful and smooth transition. https://bit.ly/3Vxc1Pt And if you’re interested in hearing more success stories and tips from other biopharmas on making the switch to a new EDC, join us at the Veeva R&D and Quality Summit, US, Sept. 9-10 in Boston. https://bit.ly/3xZFXvp   #clinicaldatamanagement #pharmaceuticals