08.20.25 -- As Billions Of Dollars Pour In, Do CDMO Valuations Matter?

Join Bend Bioscience for an insightful webinar on controlled release (CR) formulations—designed to optimize drug performance, enhance patient compliance, and reduce dosing frequency. Learn how to streamline CR development using efficient polymer screening methods and real-world case studies. Don’t miss this opportunity to gain actionable strategies and elevate your formulation expertise. Register now! Click here to learn more.

Here, we conduct a comprehensive analysis of diverse PROTAC (Proteolysis Targeting Chimeras) structures, evaluating their calculated physicochemical properties to identify key trends.

Discover how life science manufacturers are supported in digital transformation, offering solutions for automation, data integration, and compliance to optimize operations.

Conducting solid form screening early can help your team select and isolate the ideal lead polymorph to ensure manufacturability and stability while avoiding costs and hiccups down the road.

Each month, Outsourced Pharma works in conjunction with PharmSource, part of GlobalData, to present its “Contract Manufacturing: Opportunities and Threats (CMOT) Report” to our readers. The report identifies CDMOs that might be impacted by key events, including company acquisitions, product acquisitions and licenses, product approvals, late clinical product terminations, and FDA rejections.

To help manage impurities and mitigate risk across all stages of development, consider the benefits of working with a CDMO that has robust chemistry understanding and manufacturing experience.

A healthcare manufacturer facing space constraints and regulatory pressures outsourced their stability storage needs to another company, resulting in reduced costs and focus on core competencies.

Discover a solution that, in terms of integration, is setting standards with a unique compact modular design for VFFS (Vertical Form Fill and Seal) and HFFS (Horizontal Form Fill and Seal) machines.

Learn more about ready-to-use nested vials that meet the regulatory industry standards and offer broad compatibility with various fill/finish equipment available in the market.

Explore the latest trends in sustainable living and guarantee the proper handling of your clinical materials to cover everything from warehousing and distribution to returns, collection, and destruction.

Understand how free trade zones work, and explore a flexible and cost efficient way to supply clinical trials in China and around the globe.