CRO change orders can quickly become difficult to manage once a study is underway, especially when budget revisions, approvals, comments, and financial projections are spread across emails, spreadsheets, and disconnected systems. Join Clin.AI Founder and President Kalyan Obalampalli and clinical operations executive Leticia Tarilonte for a discussion on how sponsors can improve visibility into change...
July 26-30, 2026 Anaheim Convention Center Anaheim, CA, USA Speak your mind. Now accepting abstracts - inspire a global lab med community with your brilliance at #ADLM26. Accepted presenters will be part of a globally acclaimed scientific program. ADLM 2026 (formerly the AACC Annual Scientific Meeting & Clinical Lab Expo) is a program of the Association for...
Pediatric gene therapy is rapidly reshaping what is possible for children born with rare genetic diseases. Join Dr. Rachel Abu Taleb, Medical Director, Medical Affairs at Veristat, for a look at the platforms driving clinical progress, including AAV vectors, lentiviral approaches, and CRISPR-based gene editing. Through examples such as Luxturna, Zolgensma, Casgevy, and Lyfgenia, this...
Benefit from Exceptional Opportunities for Professional Development, Substantive Legal Discussion, and Valuable Networking ACI’s Summit for Women Leaders in Life Sciences Law is dedicated to providing the invaluable opportunities for networking and collaboration with the chance to meet, engage with and learn from over 300 attorneys and executives from the biotech, pharmaceutical, and medical device industries...
This expert panel will discuss how digital documentation is reshaping inspection readiness. Panelists will explore the role of electronic batch records, integrated quality systems, and automated workflows in supporting compliance with ALCOA+ principles, while enabling real-time visibility and faster audit response.
Looking for fill-finish manufacturing capacity? This webinar brings together leading CDMOs to showcase their latest sterile filling, lyophilization, and advanced packaging capabilities, along with current facility availability and timelines. Gain valuable insights into quality, regulatory compliance, and manufacturing options to help identify the right partner for your biopharmaceutical development and commercialization needs.
Explore the latest large molecule manufacturing capabilities from leading CDMOs in this informative webinar. Learn about advances in cell line development, fermentation, purification, process optimization, and scale-up, while gaining insight into available capacity, facility locations, and timelines. Whether you're evaluating manufacturing partners or planning future biologics production, this session offers a practical overview to help...
As cell therapies advance toward commercial-scale manufacturing, developers can face increasing pressure to balance performance, scalability, and process flexibility. Flexible modular workflows are emerging as a powerful approach for scalable cell therapy manufacturing, enabling enhanced process control, workflow adaptability, and operational efficiency while maintaining consistency across the manufacturing pipeline. These advantages can be particularly valuable...
Technology transfers can introduce risk and create knowledge gaps at every stage of development, whether it’s moving a process from development to manufacturing, transferring methods between analytical labs, or onboarding a new CDMO partner. This is especially true in the development of antibody-drug conjugates (ADC), where the complexity of conjugation processes, analytical characterization, and specialized...
Moving promising research from the university lab to the CDMO suite requires more than breakthrough science—it requires the right documentation, development strategy, and manufacturing readiness. In this Outsourced Pharma Live discussion, industry experts explore how academic innovators and CDMOs can better align earlier, build stronger technical packages, and create a smoother path to outsourced development...
