Drug Development Solutions

  1. Lyophilization And Sterile Manufacturing 5/5/2022

    The addition of global Sterile Fill-Finish and extensive lyophilization capabilities ensures that we are able to build on our enviable reputation and deliver on our promise of delivering life-changing therapies to patients worldwide.

  2. Drug Substance Synthesis And Manufacturing 3/3/2022

    We take an agile and flexible approach with our customers programs, offering bespoke drug substance synthesis and manufacturing, helping to accelerate molecules from candidate selection to clinical proof-of-concept and onwards towards commercial scale.

  3. End-To-End Services In Contract Manufacturing 6/9/2025

    Discover how flexible, high-quality manufacturing solutions support biopharma innovation and help bring effective therapies to patients around the world.

  4. Pre-Formulation And Material Sciences 3/3/2022

    Our formulation development and material sciences experts have over 30 years’ experience in pre-formulation and solid state characterization.

  5. Immunogenicity Testing Evolved 5/20/2024

    The success of protein-based drugs hinges on identifying potential immune system reactions early in development. Learn about an immunogenicity testing technology that offers unparalleled sensitivity.

  6. Biologics Services 4/29/2024

    Access a comprehensive suite of biologics testing services meeting cGMP standards, covering characterization, biosafety, and quality control release testing.

  7. Manufacturing GTP And GMP 3/21/2024

    Learn how a one-stop solution for your cell therapy needs can help ensure efficiency, cost-effectiveness, and faster patient treatment. Our Draw-to-Thaw® service streamlines the entire process.

  8. Microbial CDMO Services

    With over 30+ years’ of experience in microbial CDMO services, one of our core areas of expertise is the development of large-scale processes for recombinant protein expression in microbial hosts (E.coli, P.pastoris and S.cerevisiae).

  9. SMART First Human Dose (FHD)

    A CDMO with the right team of experts can aid drug development, regulatory compliance, and clinical trial supply, accelerating timelines to first human dose clinical trials and the path to market.

  10. Services For Advancing mRNA-LNPs From Bench To Clinic 2/27/2023

    Discover a one-stop-shop for LNP technologies that provides access to expertise in formulation and analytics for successful outcomes for payload and target applications. Explore end-to-end biopharma services and systems.