Drew Garty invites you to Veeva R&D Summit

Veeva Systems Inc

/@VeevaSystems

Published: August 20, 2019

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Insights

This video serves as a personal invitation from Drew Garty, a key figure at Veeva Systems, urging industry professionals to attend the annual Veeva R&D Summit. The primary goal of the message is to highlight the strategic value of the event for leaders in the pharmaceutical, biotech, and medical device sectors—specifically those involved in clinical, regulatory, quality, and IT functions. Garty emphasizes that the summit is not merely a series of presentations but a critical forum for discussing emerging best practices, exploring cutting-edge innovation areas, and engaging directly with the future trajectory of the Veeva platform.

A central theme promoted by Garty is the opportunity for attendees to gain an "inside track" into Veeva’s strategic development via the dedicated roadmap session. This session is positioned as essential for understanding Veeva’s prioritization of business problems and the thinking behind their future product development. Crucially, Garty encourages attendees to actively challenge this thinking, positioning the summit as a collaborative environment where customer feedback directly influences the evolution of the Veeva ecosystem. This interaction is vital for consulting firms and technology providers who need to align their custom solutions and implementation strategies with the vendor's future direction.

Beyond formal sessions, the speaker stresses the unparalleled networking opportunities available at the summit. He describes the event as a chance to engage in "meaningful conversations with industry colleagues," fostering collaboration and knowledge exchange among life sciences leaders. Furthermore, Garty specifically plugs a session titled "The Richard and Drew Show," which is dedicated to exploring how Veeva Vaults can solve current and near-future business challenges. This session is particularly focused on addressing CDMS business problems (Clinical Data Management Systems), indicating a strong focus on clinical operations and data management efficiency, which are core areas for AI-powered optimization and regulatory compliance within the life sciences sector. The comprehensive nature of the summit, covering clinical, regulatory, quality, and IT, confirms its importance as a holistic view of the R&D technology landscape.

Key Takeaways: • Veeva Roadmap Insight: The dedicated roadmap session offers a crucial opportunity to understand Veeva’s internal prioritization of business problems and their planned technological solutions. This foresight is invaluable for consulting firms needing to anticipate platform changes and align their custom AI and software development services accordingly. • Direct Influence on Product Development: Attendees are explicitly invited to challenge Veeva’s thinking during the roadmap session, providing a direct channel for influencing the platform's future features and ensuring that upcoming releases address specific, high-priority client needs in areas like regulatory compliance and clinical data management. • Focus on Veeva Vaults and CDMS: The highlighted "Richard and Drew Show" session confirms a deep dive into the capabilities of Veeva Vaults, particularly in solving Clinical Data Management System (CDMS) challenges. This indicates that operational efficiency, data integrity, and streamlining clinical processes are major focus areas for Veeva's R&D strategy. • Strategic Networking Opportunities: The summit is positioned as a premier venue for meaningful conversations with industry colleagues, offering unparalleled access to potential clients, partners, and key decision-makers across clinical, regulatory, quality, and IT departments within the life sciences ecosystem. • Innovation and Best Practices: The event features an exceptional lineup of industry leaders discussing new and emerging best practices and innovation areas. This provides a critical mechanism for staying current on industry trends, especially concerning the integration of advanced technologies like AI/LLMs into regulated R&D workflows. • Comprehensive R&D Scope: The summit’s coverage spans clinical operations, clinical data management, regulatory affairs, quality management, and IT strategy, confirming its relevance as a holistic learning environment for all aspects of pharmaceutical R&D technology utilization. • Customer Case Studies: The event promises over 65 breakout sessions featuring customer case studies. These real-world examples offer practical insights into successful Veeva implementations and highlight specific business problems that have been solved using the platform, providing valuable reference material for consulting engagements.

Tools/Resources Mentioned:

  • Veeva Vaults: The core platform suite discussed for solving R&D and CDMS business problems.

Key Concepts:

  • CDMS (Clinical Data Management System): Refers to the systems and processes used to manage data generated during clinical trials. The focus on solving CDMS business problems highlights the need for improved data quality, integration, and efficiency in clinical operations, areas ripe for AI and data engineering solutions.
  • Veeva R&D Summit: An annual gathering focused on technology, innovation, and best practices across the clinical, regulatory, and quality functions within the life sciences industry.