Join this webinar to learn how an integrated CDMO+CRO model is transforming bioconjugate development by reducing risk and accelerating timelines from discovery to GMP supply. Discover actionable strategies and real-world insights to streamline your ADC and biologics programs while avoiding costly delays and late-stage failures. You'll leave with insights on: - How an integrated development...
Learn how to transform your gene therapy program management by adopting the OneTeam™ approach to create a transparent, integrated “single source of truth” that replaces fragmented reporting and improves decision-making. Explore how enhanced visibility, standardized governance, and a shared digital interface can strengthen sponsor-CDMO collaboration and turn outsourcing from a black box into a streamlined,...
A 2-hour virtual expo for clinical teams to discover and compare leading patient recruitment and engagement partners—without the time, cost, or travel of traditional conferences. Choosing the right supplier impacts enrollment timelines, diversity goals, and site experience. This showcase helps you evaluate multiple options in one sitting. What to expect: ✔ Live 15-minute capability presentations...
This advanced webinar will focus on practical learnings to improve CCS outcomes. It has become clear that three stages of CCS preparation lead to a fully compliant live document that continues through the product life cycle. This session addresses operational challenges and regulatory expectations across sterile manufacturing, ATMPs, early-phase products, and CDMO environments. An interactive...
The International Research Conference is a federated organization dedicated to bringing together a significant number of diverse scholarly events for presentation within the conference program. Events will run over a span of time during the conference depending on the number and length of the presentations. With its high quality, it provides an exceptional value for students,...
Join this webinar to discover how variability reduction programs and animal-free peptones can optimize cell culture media for improved biotherapeutic yield, quality, and cost control. Learn from real-world case studies how reducing raw material variability can enhance consistency, minimize risk, and drive efficiency across your manufacturing process. Key learning objectives: - Demonstrating the value of...
More than ever, great life science startups need extensive investor connections to be successful. That’s why BioLabs joins forces with key local ecosystem partners — drawing on our international network of investor relationships — to bring the money and the talent together. Philadelphia’s third annual Investor Day event will bring together life science investors from...
Personalized cancer vaccines (PCVs) are reshaping immuno-oncology. However, translating these therapies into the clinic remains challenging. The progress is often slowed by critical bottlenecks – from suboptimal delivery, limited access to novel lipid nanoparticle (LNP) formulations, to a lack of manufacturing technologies designed for small-scale clinical production. This webinar explores how optimized ionizable LNP formulations...
In late 2025, Tufts CSDD and CRIO conducted a survey among a global community of investigative sites to better understand how sites translate clinical trial protocols and related information into practical tools such as template source documents, study plans, calendars, worksheets and shadow charts for the purposes of ensuring compliant, efficient, and high-quality data collection....
Watch leading CDMOs share their current capabilities, facility locations, and timelines - to help you identify options for your development and manufacturing needs. What can you expect? - Short, digital presentations to give you an inside look at the available capacity of industry suppliers. You will have the opportunity to ask questions of each CDMO...
