Join us for a practical discussion on selecting the right Container Closure Integrity Testing (CCIT) method for your container system. Learn how deterministic and probabilistic approaches compare, understand the impact of package design and product characteristics on method selection, and gain a risk-based framework for justifying your CCIT strategy to regulators.
Breakthrough Tech. Expert Insights. Real-World Impact. 400+ diagnostics professionals from across the industry 120+ speakers leading innovation in clinical and molecular Dx 6 highly focused tracks spanning emerging technologies and commercial strategy Unmatched networking with partners, labs, regulators, and investors Emerging company spotlight with novel platform technologies Next Generation Dx Summit is where the diagnostics...
Philly biotechs and emerging startups, join Mispro and B+labs for breakfast and a behind-the-scenes look at the research spaces available at Cira Centre. If you’re launching preclinical R&D in the next 6–12 months or currently outsourcing your program to a CRO, this is an opportunity to learn how co-working incubator and contract vivarium space, along...
Achieving consistent upstream performance remains a critical challenge as bioprocesses become more complex and quality expectations continue to rise. From variability in raw materials to maintaining cell growth, productivity, and product quality across platforms, process developers are under increasing pressure to build more robust and reliable manufacturing processes. Join this webinar to explore practical strategies...
Explore data from an end-to-end CAR-T workflow using cryopreserved leukopaks. This session will examine how key process parameters affect cell recovery, viability, consistency, and scalability across washing, cryopreservation, thawing, and final formulation. Attendees will learn practical strategies for defining operating ranges, reducing variability, and building more robust closed-system autologous manufacturing workflows.
Join experts from Dr. Vince Clinical Research, along with moderator Polly Dawkins of the Davis Phinney Foundation, for a practical discussion on designing and executing successful Parkinson’s disease clinical trials. The session will explore symptomatic and disease-modifying study designs, endpoint selection, emerging research trends and operational challenges. Attendees will gain real-world insights to help advance...
MEDevice Boston, by Informa, brings together leading medical device OEMs, startups, and suppliers from New England and beyond into a MedTech event engineered to advance the industry. Intentionally designed for partner connections and supplier evaluation, this two-day experience creates a focused environment where high-intent buyers and solution providers connect. Through curated networking, hands-on learning, and...
A practical framework for reducing variability, minimizing manual sampling, and improving run-to-run consistency with modern UF/DF control strategies. August 26, 2026 | 11:00 AM ET Ultrafiltration Diafiltration (UF/DF) is often treated as a straightforward concentration and buffer-exchange step, but teams know the reality looks different. Small differences in setup, endpoint definition, and in-process decision-making can...
Every vivarium faces similar pressures and challenges, but not every team solves them the same way. In this session, we’ll highlight how organizations like yours are overcoming common challenges in staffing, colony support, workflow execution, and compliance. Through real-world examples, you’ll gain insight into the decisions, tradeoffs, and strategies that helped these teams operate more...
Are you making the most of your time at CPHI Milan? Watch this free virtual event to evaluate CDMOs, CMOs, API suppliers, packaging providers, and other outsourcing partners before you arrive onsite. Gain early insight into supplier capabilities, compare potential partners, and build a focused meeting strategy that maximizes your time at CPHI Milan. Register...
