In this free webinar, uncover practical strategies for achieving accelerated clinical trials without sacrificing quality or compliance. Attendees will learn why emphasizing quality from the outset prevents late-stage issues that can derail timelines, ensuring a smoother path to market. The featured speakers will discuss how implementing a proactive, risk-based approach through frameworks identifies and eliminates bottlenecks, driving efficiency without compromising rigor. Attendees will gain insight into how harnessing advanced data analytics enables real-time monitoring and decision-making, accelerating study timelines and enhancing data integrity.
TORONTO, July 9, 2025 /PRNewswire-PRWeb/ -- In the high-stakes world of clinical research, the prevailing belief is that speed and quality are mutually exclusive — yet achieving accelerated clinical trials doesn't have to come at the expense of rigor.
This webinar will demonstrate how integrating quality into every phase of clinical development can not only prevent costly delays but also serve as a catalyst for faster, more reliable outcomes.
Drawing on real-world examples and industry expertise, the featured speakers will explore how early collaboration with a trusted CRO partner, adherence to Quality by Design principles and the strategic use of data and AI can transform quality from a bottleneck into a competitive advantage — ultimately paving the way for a more accelerated clinical trial process.
Join the speakers to explore how:
- Quality can become a catalyst for faster, more reliable clinical trials
- Early CRO/CDMO collaboration helps maintain momentum and reduce costly rework
- Proactive design, data and AI work together to eliminate delays and strengthen compliance
Register for this webinar to uncover practical strategies for achieving accelerated clinical trials without sacrificing quality or compliance.
Join Valerie Brown, Senior Vice President, Quality, Enterprise Learning & EHS, Thermo Fisher Scientific; Robin Kumoluyi, Vice President Global Head Quality & Regulatory, Pharma Services, Thermo Fisher Scientific; and Helen J Neal, Vice President, Global Head Clinical Operations, , for the on Tuesday, July 29, 2025, at 11am EDT (4pm BST).
For more information, or to register for this event, visit .
ABOUT XTALKS
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars and digital content to the global life science, food, healthcare and medical device communities. Every year, thousands of industry practitioners (from pharmaceutical, biotechnology, food, healthcare and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps professionals stay current with industry developments, regulations and jobs. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
To learn more about Xtalks visit
For information about hosting a webinar visit
Media Contact
Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, [email protected],
SOURCE Xtalks
Share this article