How can sponsors, CROs, and sites adapt to improve enrollment and retention in a changing clinical trial environment? The Partnerships with Sites Summit challenges how sponsors, CROs, and sites adapt to a rapidly evolving clinical trial ecosystem shaped by shifts in the global site landscape, increasing study complexity, evolving technology, and changing operating models. These...
The Charles River Biotech Symposium unites drug development professionals in an interactive setting to discuss the nonclinical development of biotherapeutics, including regulatory issues and innovative approaches to problem-solving. The collegial spirit of this meeting creates exceptional opportunities for information sharing and networking. Register today to save your seat for an event aimed to inspire, educate,...
Join us for an exclusive webinar exploring practical strategies to improve therapeutic antibody manufacturing through integrated upstream and downstream process solutions. As therapeutic antibody titers continue to rise, manufacturers face increasing pressure to remove harvest bottlenecks, improve purification efficiency, and maintain product quality while controlling manufacturing costs. Successfully integrating upstream and downstream operations has become...
As the December 1, 2026 release of the revised USP <87>, Biological Reactivity Tests, In Vitro, approaches, pharmaceutical and medical device manufacturers should begin evaluating how these changes may impact their material qualification, biological evaluation, and compliance strategies. While the final chapter has not yet been published, the proposed direction reflects a broader industry shift...
Connecting 1,000+ Industry Executives, Innovators, and Change-Makers The 16th Annual DPHARM® will offer an unparalleled opportunity to hear senior clinical operations executives and innovative thought leaders unveil the latest innovations on modernizing clinical trials. DPHARM speakers report on R&D industry innovation that drives greater efficiencies and accelerates clinical trials for the benefit of patients. DPHARM 2026 features...
The 12th Annual BioHealth Capital Region Week returns September 15–17, 2026, at US Pharmacopeia in Rockville, Maryland, bringing together leaders from industry, academia, government, investment, and entrepreneurship for three days of programming, networking, and regional collaboration. This year’s theme, “Growing the BioHealth Capital Region of Tomorrow,” reflects the work needed now to strengthen commercialization, expand...
A risk-averse investment climate has made it more difficult for startups to find the funding needed to bring novel treatments into the clinic. However, alternative funding sources, investment models, and nontraditional investors are stepping in to fill the void. Our panel of experts will identify and discuss new funding opportunities and strategies for companies at...
Virtual Pharma Expo - a themed event featuring presentations and demonstrations by leading experts from pharmaceutical equipment providers for oral solid dose manufacturing and packaging.
Innovations in self-administered and wearable drug delivery technologies promise convenience but bring questions about how to effectively monitor and manage patient safety, adherence, dosing accuracy, and, ultimately, medical outcomes. In this live online session, expert panelists will discuss approaches to leveraging the power of digital tools to provide feedback loops and administrative controls. From both...
Transitioning development processes into GMP manufacturing can come with a fair share of growing pains. Development teams need to contend with things like sourcing and validating new materials, ensuring regulatory compliance, performing risk assessments, and evaluating facility fit. Unexpected challenges in any aspect of this transition can be costly and delay a product’s time to...
