02.04.26 -- End‑To‑End Development, Analytics, And Manufacturing Solutions

Explore global CDMO capabilities that streamline drug development and manufacturing, leveraging advanced infrastructure and regulatory expertise from early formulation through commercial production.

Pedro Morales, Director, Scientific Advisor of Biologics Analytical Services, explores how Catalent delivers tailored solutions through deep expertise and advanced capabilities.

An award-winning managed service provider that places its people at your site to run and manage manufacturing and laboratory services, eliminating headcount, co-employment, and project-management concerns.

Accelerate your biopharma journey with a comprehensive service portfolio designed to speed development, reduce costs, and minimize risk from molecule to market.

Uncover how Integrated Unprocessed Bulk testing — including viral assays, NGS, and TEM — can safeguard product safety, minimize contamination risks, and streamline biologics development.

Our state-of-the-art labs and advanced analytical tools enable efficient route scouting, faster process development, and optimized reaction conditions for scaling materials used in toxicology studies and cGMP clinical and commercial production.

Our team of analytical experts provides experience, efficiency, and technical proficiency in the development/validation of analytical methodology and GMP testing support for your project.

Move drug development into the modern era with a CRO that offers assay development and validation, bioanalytical testing, sample prep, and more. Explore why choosing us is a smart decision for accelerating bioanalysis.