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From evolving strategic partnerships to emerging technologies and supply chain resiliency — learn how CDMOs are adapting to the new OSD manufacturing playbook.
By: Charlie Sternberg
Water for injection (WFI) sits at the heart of injectable drug manufacturing.
Released By ROIS CDMO
Ensuring quality, compliance and patient-centric operations with robust processes and innovative solutions.
By: Barry Kay
Looking at the critical challenges of developing bispecific antibodies, and how the use of comprehensive tailored approaches can enhance their productivity, stability, quality, and more.
By: Sherry Gu
Hovione’s chief executive shares his vision for establishing and maintaining leadership as a CDMO.
From Challenge to Breakthrough: Driving Speed and Quality in BsAb Development
The Rising Strategic Power of LQPPVs in AI-Enabled Pharmacovigilance
Powering Patient-Centric Delivery: How Partnerships Are Transforming Fill-Finish Services
AI Data Security: The 83% Compliance Gap Facing Pharmaceutical Companies
As increasing trial complexity becomes a regulatory risk, sponsor expectations of CROs and data partners are changing.
By: Kristin Brooks
How technology, data, and collaboration are reshaping pharma distribution to protect patient access.
By: Chris Van Norman
What defined pharma in 2025? Contract Pharma’s most‑viewed breaking news offers insights.
Subscribe to Magazine for top news, trends & analysis
Evotec team shares insight on addressing solubility and bioavailability challenges for today’s complex molecules.
Released By EVOTEC
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
Pfizer
Merck
Johnson & Johnson
Abbvie
AstraZeneca
Roche
Novartis
Bristol Myers Squibb
Lilly
Sanofi
Outlining four developments set to change how life-sciences organizations design, deploy, and govern intelligent systems in the year ahead.
By: Doron Sitbon
Regulatory momentum, device innovation, and advances in formulation science are repositioning the nasal route as a strategic option for systemic and CNS therapies—provided sponsors address translational and development challenges early.
By: Ted Barrett
A look at the biologics, gene therapies, and vaccines most likely to reshape care —and manufacturing—in the year ahead.
By: Adam Tuszyner
How Coperion’s single-source approach helps CDMOs and pharma manufacturers reduce complexity, accelerate scale-up, and support both batch and continuous operations.
Released By Coperion
How Ropack’s evolution from service provider to strategic CMO partner reflects broader shifts in manufacturing, packaging, and quality expectations.
Released By Ropack Pharma Solutions
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
When planning a technology transfer, choosing a CDMO partner with deep scientific, operational, and cross‑functional expertise can make all the difference. In this expert panel discussion, Rentschler Biopharma’s experts share real‑world lessons from supporting complex programs through phase‑appropriate development, scale‑up, and cGMP manufacturing. They offer a transparent look at what truly drives a smooth, efficient, and reliable tech‑transfer experience.
Key Insights:
Core scientific and operational considerations as processes advance to cGMP production.
How early alignment, molecule understanding, and process robustness reduce downstream complexity and risk.
Practical insights into where transfers commonly encounter challenges—and how experienced teams plan ahead to mitigate them.
How clear planning, cross functional coordination, and predictable scale-up contribute to reliable timelines and overall project success.
Why attend?
Whether this is your first tech transfer or you’re optimizing a new phase of development, this panel offers grounded, experience driven guidance that can help you prepare effectively. Expect real examples and practical takeaways you can directly apply to your next transfer.
Sponsored By Rentschler Biopharma
Polymer-based excipients, including lactide-glycolide and lactic acid-glycolic acid polymers (PLGs and PLGAs, collectively referred to as LG polymers), play a vital role in enhancing controlled drug release, delivery and bioavailability—particularly in long-acting injectable (LAI) formulations. While these excipients offer multiple benefits, the industry faces challenges in excipient selection due to naming differences, formulation complexity, and raw material variability.
Join this webinar as USP experts take a deep dive into standards and solutions that support quality and performance across the drug lifecycle and present:
By showcasing this integrated strategy, USP aims to empower stakeholders with these standards and solutions to navigate the complexities of excipient naming, selection and characterization for LAIs.
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.
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
The financing was “significantly” oversubscribed, underscoring investor belief in LEON’s proprietary technology.
By: Patrick Lavery
Immuno-oncology portfolio sales drive growth in the quarter.
Mounjaro and Zepbound drive significant growth in the quarter.
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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