ABOUT PHARMASOURCE
PharmaSource is the online community for drug development and outsourced manufacturing decision-makers in pharma and biotech. Through expert interviews, podcasts, analysis, and live events, including CDMO Live and the External Manufacturing Leaders think tanks, we share peer-to-peer best practices on CDMO selection, procurement, quality, and CMC strategy.
EDITORIAL CONTENT
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Pretzel Therapeutics COO Baruch Harris shares creative financing strategies, from spinouts to non-dilutive funding, that keep biotech companies alive when VC capital dries up. Access the full conversation to build your capital roadmap.
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U.S. funding cuts could leave 75 million children without routine vaccines. Five supply chain leaders explain what resilience actually requires and what's at stake if the sector fails to act.
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Sanofi's Manda Pasarkar shares 20+ years of regulatory CMC expertise, covering FDA, EMA, and PMDA differences, CDMO partnerships, ICH guidelines, and AI's emerging role in global drug approvals.
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Tariffs, FDA workforce cuts, and a stalled BioSecure Act are reshaping CDMO strategy. Get the full policy breakdown to stress-test your supply chain planning now.
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Sid Jain's two decades across Novartis, Regeneron, and Sanofi reveal six CMC strategies redefining how biologics reach the clinic, from CDMO selection to digital transformation pitfalls.
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U.S. pharma can't reshore what domestic capacity can't absorb. Senior leaders from Takeda, Biogen, Eli Lilly, and others reveal why tariff pressure is colliding with a sterile fill-finish shortage, workforce gaps, and ADC capacity bottlenecks.
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112 pages of executive insight from CDMO Live Europe 2026: tariffs, geopolitics, supply resilience, AI in manufacturing, and why strategic partnerships remain aspirational for most.
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Senior pharma leaders from Pfizer, Bayer, BioNTech and others debunk dual sourcing myths and reveal what separates strategic CDMO partnerships from transactional ones.
CONTACT INFORMATION
PharmaSource
210 W Kensinger Dr Suite, 500
Cranberry Twp, PA 16066
UNITED STATES
Contact: Dora Wells, Editor
THOUGHT LEADERSHIP
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Learn how to best align your development strategy, guide cross-functional decisions, and build a clear pathway from discovery to successful commercialization.
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Early decisions can have long-lasting consequences for development timelines, cost, risk, and overall probability of success. Engaging the appropriate disciplines early helps avoid downstream surprises and rework.
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Only 6.7% of Phase 1 drugs reach approval. A well-structured Drug Development Plan (DDP) can meaningfully improve your odds — learn exactly how to build one.