Formulation Development Solutions

  1. Empowering Biologics Development With HRMS Services 7/3/2025

    Examine ways to accelerate biologic development with high-resolution mass spectrometry services that deliver precise, reliable data from discovery through commercial release.

  2. Your End-To-End CDMO Partner

    Partner with a trusted, globally proven CDMO whose world-class, rapidly scalable facilities and unwavering commitment to quality help accelerate patient access to life-saving biologics.

  3. Bioprocess Courses And Services 8/5/2022

    Learn how our courses and services provide access to science experts that will guide your process and engineering needs and suggest optimization strategies to support an efficient scale-up of the process.

  4. RNA 9000 Purity & Integrity Kit 5/10/2022

    Easily analyze a diverse array of RNA species, from 50-9,000 bases, and achieve high-resolution data with a purity & integrity kit.

  5. Which Organ-Chip Design Is Right For You? 10/15/2024

    Explore detailed product specifications and utilize a helpful decision tree to determine which organ-chip best meets the needs of your research.

  6. Discovery Hybrid Rheometers: Temperature Systems And Accessories 4/6/2023

    Explore a wide variety of DHR temperature systems and accessories, designed for superior performance and ease-of-use.

  7. Eliminate Doubt With Chemistry Technical Services 7/7/2022

    The Waters Chemistry Technical Service team that can assist with recommending products for development methods, guidance in optimizing conditions for established methods, to troubleshooting any deviation from expected analytical outcomes.

  8. Drug-Drug Interaction (DDI) Studies 10/16/2023

    Learn how an innovative development platform with the unique ability to fully integrate DDI studies accelerate timelines and improve the likelihood of downstream success.

  9. Where Expertise Meets Simplicity: BD PartnerPath™ Program 8/12/2021

    The commercialization of a combination product can be a complex process that involves obtaining the proper data, choosing a drug delivery system, developing a regulatory strategy and conducting clinical trials—all of which can increase development risks and affect your molecule’s time to market.

  10. From Process Development To QC—Optimize Your mAbs Workflow 5/29/2026

    See how integrated analytical capabilities help improve visibility across mAb workflows, enabling faster decisions, stronger process control, and reliable quality outcomes from development through QC.