Events

Selecting the right CRO is one of the most critical decisions in clinical development, yet rarely a straightforward one. Sponsors often find that comparing CRO proposals isn’t an apples-to-apples exercise — with variations in assumptions, timelines, and resource structures making true comparisons difficult. This session draws on insights from more than $2B in CRO selections...

AAV vectors offer clear benefits for gene therapy, and continued advances in technology have increased target specificity, improved potency, and intensified production efficiency. Even with significant attention early in development, analytical activities for gene therapy often land on the critical path. This webinar provides considerations for phase-appropriate AAV characterization and release activities from pre-clinical to...

We are very excited to invite you to our BVS Holiday Biotech Community Event - an evening of celebration, networking, and festive cheer! Mark your calendars for a great opportunity to connect with industry leaders, explore innovative products, and mingle with fellow professionals in the biotech community. This special event is designed exclusively for all...

This webinar explores the latest advancements in RNA manufacturing, with a particular emphasis on the scalability of production processes. Special attention is given to capping strategies, highlighting their critical role in ensuring RNA stability and translational efficiency at industrial scales. Attendees will gain insights into current challenges and innovative solutions for optimizing capping processes in...

Cleanrooms hosting pharmaceutical manufacturing operations are inspected at a critical scale to ensure compliance to regulatory standards. With this comes a responsibility to the manufacturing operations, quality, facility maintenance groups and the design professional team to provide a pathway to achieve regulatory approval. We will explore critical lessons from FDA 483 observations and Warning Letters...

This webinar will explore multiple perspectives on whether study sponsors should provide standardized, study-specific eSource templates to investigative sites. Attendees will examine practical implications, legal and regulatory considerations, and the distinct advantages and challenges from both sponsor and site viewpoints. Through structured debate and expert insights, participants will gain clarity on this complex operational and...

Join W.L. Gore & Associates Application Specialist David Kunzig to explore the critical role of venting and microfiltration in life science applications, from infusion, drug delivery, surgical suction, negative pressure wound therapy, diagnostics, hemodialysis, eye surgery, urology, and ostomy. Discover how vent orientation and placement can make or break system performance, using relatable analogies and...

Launch-ready & peak-proof: Discover how to bridge packaging gaps and act as a reliable backup during demand surges. You’ll learn how manual precision at an industrial scale ensures seamless transitions to automated packaging, and why this approach is a game-changer for accelerating product launches.

As cell and gene therapy (CGT) advances, regulatory expectations around product quality and manufacturing rigor continue to rise—especially in viral vector production. One emerging challenge is the need to demonstrate clearance of residual reagents used during upstream processing, a requirement increasingly emphasized by regulatory agencies like the FDA. In this webinar, Miguel Dominguez and Lloyd...

As genetic medicine advances toward targeted in vivo delivery, developers face new challenges in translating promising concepts into clinical reality. From payload design to conjugation chemistry and analytics, each decision shapes manufacturability, scalability, and regulatory success. In this webinar, experts from Cytiva will share five practical considerations for teams advancing targeted in vivo LNP programs...