Drug Development Solutions

  1. PBPK Predictive Modeling Services

    Early identification of potential absorption risks is critical for rapid and efficient drug development. Lonza's PBPK modeling services are designed to de-risk your drug development program.

  2. 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.

  3. Advancing Nitrosamine Testing For Evolving Regulations 6/10/2025

    Explore how specialized analytical expertise and advanced instrumentation enable precise nitrosamine testing to help drug developers meet strict and evolving regulatory requirements.

  4. Advancing Lyophilization Through Formulation, Process Development 1/21/2026

    Lyophilization development and modeling improve stability, streamline freeze‑drying cycles, reduce risks, and support efficient advancement of sensitive formulations.

  5. Microbiology Testing: Health Inspired, Quality Driven 4/22/2024

    Whether driven by regulatory mandates or the need to maintain sterility, our services can assist you in meeting these requirements efficiently and accurately, thereby safeguarding patient well-being.

  6. Scalable Manufacturing Of Sterile Drug Products 3/31/2023

    Discover comprehensive clinical to commercial scale manufacturing services that deliver true life-cycle management for sterile drug products that bring treatments to patients with efficiency and quality.

  7. High Resolution Mass Spectrometric Analysis Of Complex Biotherapeutics 5/7/2025

    Understand why continued research and collaboration between industry and regulatory bodies are essential to define guidelines that ensure safety and efficacy in this rapidly advancing field.

  8. Reduce Costs, Increase Efficiencies, And Improve Development Pipelines 4/29/2024

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

  9. European Center Of Excellence For Clinical Biologics

    Explore how our proven expertise and simplified execution with development, filling, and analytical under one roof ensure safe, efficacious products reach patients in need.

  10. Cleanroom Capabilities And Expertise

    Learn how the right partner can ensure that your facilities maintain cGMP-compliance and help establish the correct testing program and parameters based on your needs.