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Video | Life Science Leader | On this week's episode of the Business of Biotech, Alex Aravanis, M.D., Ph.D., CEO of Moonwalk Biosciences, talks about the opportunity in obesity beyond GLP-1s. |
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Guest Column | By Karen Zhu, Ph.D., Austin Jeffries, Ph.D., and Erin Law, MS, Lifescience Dynamics | The American Diabetes Association 2026 conference showed where we are and where we're going with GLP-1 therapies. |
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Guest Column | By Zaher Nahle, Ph.D., MPA | Part 2 follows the consequences into Wall Street, asking what better evidence could mean for pharmaceutical valuations and, ultimately, drugs already in the portfolio. |
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Article | By Sam Whitaker, Mural Health, and Kelly FitzGerald, WCG | Explore the tax reporting requirements, including the threshold for payments requiring a 1099 form rising from $600 to $2,000 in 2026. |
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Article | By Mike Stratton, CSS | To preserve the quality of care and build a more effective approach to trial design, a sponsor must consider their approach to patient recruitment and enrollment early and often. |
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Poster | By Mikkal Blick, Monika Szeszel, Frank Fabian, et al., Cytiva | Discover how a platform approach to AAV manufacturing can reduce development time and cost, as well as how optimized processes enable reliable production and scalable implementation in bioreactors. |
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White Paper | By Eunbi Iris Cho, Ph.D., Samsung Biologics | ADC formulation development requires a molecule-specific strategy, balancing antibody, linker, and payload interactions while addressing stability challenges beyond traditional mAb development experience. |
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Article | Cencora | Uncover the implications of the shift to the European Medicines Agency's Pharmacovigilance System Master File (PMS) database for the pharmaceutical industry. |
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Infographic | Citeline | In 2024, the number of industry-sponsored clinical trials reaching completion accelerated significantly. Explore the trial counts and rankings, top 5 diseases for trials, and more. |
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E-Book | BioPhorum | See how AI can be safely and effectively deployed in regulated pharma environments, with practical guidance on risk, governance, and lifecycle management rooted in GAMP 5 principles. |
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