01.30.26 -- A Serial Biotech Entrepreneur's Recipe For Success

AI has great potential to enhance the efforts of your team members by accelerating data interactions. Watch this webinar and discover how AI can improve clinical trial outcomes and data management.

Clinical research sites often face ophthalmic endpoint challenges, causing delays, deviations, dropouts, and burnout. Check out the four-step framework to overcome these issues efficiently.

Learn how leveraging the expertise and capabilities of an experienced partner is a key factor in optimizing AAV processes using Design of Experiment (DoE), thereby reducing variability and risk.

The session focuses on the use of T3P (propanephosphonic acid anhydride) in amidation and peptide coupling reactions, including both liquid-phase and solid-phase peptide synthesis.

Lentiviral vector manufacturing is complex and highly regulated, which is why a specialized CDMO is required to ensure safe, scalable, and compliant production from early development to commercialization.

Examine the critical issue of patient retention in clinical trials and six practical strategies to help CROs, biopharma companies, and clinical trial staff address these challenges.

Before you dive into clinical trials, ask yourself: Is my company operationally ready to handle the complexity? Uncover key upgrades that can help you streamline operations and reduce risk.