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Hovione’s chief executive shares his vision for establishing and maintaining leadership as a CDMO.
By: Charlie Sternberg
Ventyx is developing a pipeline of small molecule therapeutics designed to treat inflammation across a broad range of disease states with high unmet need.
Join us on January 29th for a data-driven look at the trends shaping CDMO marketing in 2026.
What defined pharma in 2025? Contract Pharma’s most‑viewed breaking news offers insights.
As small-molecule pipelines grow more complex, formulation has become a decisive factor in whether promising compounds reach patients.
Released By Bend Bioscience
Powering Patient-Centric Delivery: How Partnerships Are Transforming Fill-Finish Services
AI Data Security: The 83% Compliance Gap Facing Pharmaceutical Companies
CDMO Industry Trends 2025
CDMOs: Challenges & Opportunities in a Big Year of Change
How technology, data, and collaboration are reshaping pharma distribution to protect patient access.
By: Chris Van Norman
Contract Pharma has long chronicled the evolution of the CDMO, as seen in pieces like The Modern CDMO and CDMOs: The Cornerstone of Biopharmaceutical Innovation, yet once again the goalposts have shifted. In an industry defined by scientific advancement, regulatory pressure, and supply-chain volatility, it is natural that the definition of a “modern CDMO” is […]
By: Tom Morford
Subscribe to Magazine for top news, trends & analysis
Brian McCollum walks us through Glatt’s capabilities and technologies available at its Ramsey, NJ site from development to commercialization.
Released By Glatt Air Techniques
Jai Murthy of Actylis shares insight on overcoming supply chain fragility, buffer prep solutions, and approaches to customization.
Released By Actylis
Nigel Langley of gCHEM discusses the advantages of its high-purity Dimethyl sulfoxide in pharmaceutical applications.
Released By gChem
Pfizer
Roche
Johnson & Johnson
Amgen
AstraZeneca
Abbvie
Merck
Sanofi
Novartis
Bristol Myers Squibb
Strategies for strengthening API sourcing amid geopolitical, regulatory, and supply chain volatility.
By: Hamilton Lenox
Data management, study design, and the groundwork needed to build pharma’s digital revolution.
By: Nicolas Descamps
Navigating the shift to next-generation propellants in pMDIs by balancing environmental goals, patient care, and regulatory demands.
By: Craig Sommerville
Liliana Miinea of Lubrizol Pharmaceuticals R&D shares insight on challenges drug developers face and solutions for today’s complex drug products.
Released By Lubrizol Life Science Health
Sentry’s foreign trade zone expertise helps pharmaceutical companies mitigate risks from tariffs and global trade volatility.
Released By Sentry BioPharma Services, Inc.
Nelson Labs’ Christine Walton provides insights on newly proposed regulatory chapters.
Released By Nelson Laboratories, LLC
External regulatory, economic, and technological forces ensured that the story of 2025 for CDMO marketers was turbulence. How will marketing teams adapt in 2026?
149 marketing leaders shared their predictions and strategies in the 2026 CDMO Marketing Trends Report from Altitude Marketing. Join John Boogaard, the Senior Director of Global Marketing at Adhesives Research, Inc. and ARx Pharma., and Adam Smartschan, the Chief Strategy Officer at Altitude Marketing, in a webinar that explores the results in the report as well as their insight into both the internal strategies and industry headwinds that will shape CDMO marketing through the next year.
You’ll learn:
• Which channels generate the most qualified leads • How budgets and team structures are evolving • Where AI is delivering real efficiency gains • How external pressures are impacting marketing performance
Register now for a data-driven look at the trends shaping CDMO marketing in 2026.
The webinar will provide updates from the U.S. Pharmacopeia (USP) efforts to develop and implement standardized System Suitability Standards (SSS) for Extractables and Leachables (E&L) testing, addressing the lack of global regulatory guidance and variability in data quality. Initiated in 2021, the project involved extensive stakeholder engagement, laboratory studies, and a global round-robin study across 13 labs using GC-MS and LC-MS platforms. The standards aim to ensure instrument performance and data reliability through carefully designed compound mixtures. Based on feedback and study results, the mixtures were re-optimized and stability-tested, with plans for industry release in Q3 2026 and potential inclusion in USP General Chapter <1663>. The presentation also highlights ongoing efforts to develop standards for rubber oligomers and materials of construction (MOC), and updates to enhance the USP leachables General Chapter <1664> for various dosage forms, reinforcing USP’s commitment to enhancing patient safety and regulatory harmonization.
Join Samsung Biologics to explore how ExellenS™ delivers standardized equivalency and accelerated speed across our global manufacturing network. Leveraging integrated manufacturing control systems (MCS) and ≥95% standardized facility design, we achieve seamless scalability and reduced tech transfer timelines. With 100% on-time delivery maintained despite global disruptions, our unified platforms empower predictable outcomes for complex supply chains.
R&D Chemist and Project Manager Luca Allievi on nitration, phosgenation, and the power of DoE in sustainable process development.
Released By Valsynthese
Insight on market dynamics driving OSD forms, key development and manufacturing challenges, and the specialized capabilities needed to address them.
Released By Pfizer CentreOne
Vice President and General Manager of Pfizer CentreOne talks with Ben Locwin about drug development trends and challenges and Pfizer’s lightspeed approach.
As data volumes accelerate, AI is becoming deeply embedded in safety operations and local qualified persons for PV are emerging as anchors of oversight.
By: Ana Pedro Jesuíno
Integrating science with strategy, empathy and intelligent tech-enabled processes.
By: Debra Gerlach, Anna Haught, Megan Hooton, Raja Shankar
The intersection where science meets production is where real value is created.
By: Audrey Greenberg
Growth in the quarter driven by DARZALEX, CARVYKTI, ERLEADA in Oncology, TREMFYA and SIMPONI in Immunology, and SPRAVATO in Neuroscience.
By: Kristin Brooks
Merck 3Q Revenues: $17.3 billion (+4%) 3Q Earnings: $5.8 billion (+83%) YTD Revenues: $48.6 billion (flat) YTD Earnings: $15.3 (+14%) Comments: KEYTRUDA sales were up 10% to $8.1 billion driven by continued global demand and uptake in earlier-stage indications. GARDASIL/GARDASIL 9 sales declined 24% to $1.7 billion primarily due to lower demand in China, lower […]
Revenue in the quarter was impacted by declines in COVID-19 product sales.
Dr. Rodolfo Romañach and Dr. Rafael Méndez from the University of Puerto Rico, Mayagüez, present a stream sampler for real-time monitoring of powder blends.
By: Emil W. Ciurczak
The particle size of the API and excipients affects more than just the stability and appearance of the product.
It’s not your Mom’s way, anymore.
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