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In this webinar, SGS’s Microbiology Manager, Patricia Peron, will take a deep dive into: Stick around after the presentation for a Q&A where you will be able to submit questions.
Marken’s Mike Bartone, VP of Global Cold Chain Solutions Management, on scaling temperature-controlled precision logistics, driving innovation with Packaging as a Service (PaaS) and mastering the pace of change in the rapidly evolving clinical trial ecosystem.
Released By Marken, UPS Healthcare Precision Logistics
David King of Samsung Biologics shares insights on market demand and the technologies and capabilities needed to support today’s drug products.
Released By Samsung Biologics
Practical solutions to purification and analytical challenges in PDC manufacturing, along with insights into synthesizing complex peptides, oligonucleotides, and conjugates.
Released By NAGASE & CO., LTD.
Operational strategies to optimize efficiency and cost effectiveness, and secure an unbroken chain of custody from manufacturing to the end-user.
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
Why pharma needs automated AI security now.
By: Frank Balonis
Andrei Georgescu of Vivodyne discusses key advantages of its humanized drug testing platform and the impact of the FDA’s policy shift.
By: Kristin Brooks
Wyatt McDonnell of Infinimmune shares insight on human-first models and what the FDA’s policy shift means for biotech R&D.
Subscribe to Magazine for top news, trends & analysis
EVP & COO Todd Nelson reflects on Porton J-STAR’s defining milestones, global network strategy, and what’s ahead as the company enters its third decade.
Released By Porton
Rod Ketner on Serán BioScience’s science-first culture and what biotechs should look for in a CDMO.
Released By Serán Bioscience
Pfizer
Roche
Johnson & Johnson
Amgen
AstraZeneca
Abbvie
Merck
Sanofi
Novartis
Bristol Myers Squibb
Mark Foster, General Manager of Oliver Design, shares insights on balancing patient needs, manufacturability, and sustainability in biopharma packaging.
In this webinar, SGS’s Microbiology Manager, Patricia Peron, will take a deep dive into:
Stick around after the presentation for a Q&A where you will be able to submit questions.
This webinar provides a high-level introduction to Primary Packaging Qualification in the pharmaceutical industry. We'll take a systematic approach to qualifying packaging systems by examining four key factors: Compatibility, Safety, Protection, and Quality Control.
The session will also highlight relevant industry standards, including USP <381>, <382>, <661.1>, and <661.2>, and address common challenges encountered during the qualification process.
Whether you're new to the topic or seeking a refresher, this webinar offers valuable guidance and practical insights.
What you’ll learn by attending:
As drug developers seek out novel solutions for geriatric and pediatric populations and patients with difficulty swallowing (dysphagia), liquid suspensions have become increasingly popular. However, while liquid suspensions have distinct advantages to pills, tablets, and traditional liquid solutions for specific patient populations, their unique formulation requirements make them highly challenging to develop and manufacture.
In order to meet rising demand, CDMO partners must have the necessary expertise to accelerate liquid suspension formulation development. In this exclusive thought leadership piece, Mikart’s very own Gus LaBella, Director of Formulation Development, shares the keys to liquid suspension formulation, including:
Vice President and General Manager of Pfizer CentreOne talks with Ben Locwin about drug development trends and challenges and Pfizer’s lightspeed approach.
By: Tim Wright
Global Head of Strategic Account Management for Pfizer CentreOne talks with host Ben Locwin about the advantages of working with an integrated CDMO.
Vice President and Global Contract Manufacturing Leader for Pfizer CentreOne talks with Ben Locwin about supply chain reliability trends.
This project could reduce costs in pharmaceutical development and manufacturing.
By: Rachel Klemovitch
According to a new report, the life sciences sector accounted for 49.3% of total investment in Pittsburgh’s tech economy last year.
By: Charlie Sternberg
This deal will expand and strengthen iOncologi’s immunotherapy pipeline against solid tumors.
This acquisition strengthens Tobin Scientific’s regional footprint in New England as well as its life sciences capabilities.
This platform aims to deliver high-quality cyclic peptides with faster timelines and better economy across a broad range of therapeutic areas.
AvenCell selected ViroCell for retroviral vector CDMO services to drive its pipeline of innovative allogeneic CAR T-cell therapies.
What’s at stake in the face of enforcement deadlines and how exception management lays the groundwork for future-ready supply chains.
By: Tracy Nasarenko
Combining technology, data visualization and data expertise to enhance decision-making and efficiency.
By: Ping Chung Chang
Key regulatory trends laying the foundation for updated policies, risk-based regulatory frameworks, and forward-looking initiatives.
By: David Cameron
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