Insights On Downstream Manufacturing

  1. Back To Basics: Understanding Testing For Process-Related Impurities 1/27/2026

    Master the fundamentals of identifying and monitoring process-related impurities. Ensure biologic safety and regulatory success by optimizing your analytical strategy.

  2. Oligonucleotide Purification And Synthesis 1/27/2026

    Examine how a 21‑mer oligo was synthesized and purified through systematic resin screening, method optimization, and successful scale‑up to build reliable, high‑purity chromatography workflows.

  3. Purification And QC Of An RNA 21‑Mer Oligonucleotide Via LC‑MS 1/27/2026

    Learn how buffer choice, gradient strategy, and pretreatment steps influence recovery, purity, and resolution when purifying a native RNA oligo, with analytical confirmation and practical guidance.

  4. Scalable, Sustainable Support For Next‑Gen Primer Systems 1/27/2026

    Explore how an optimized solid‑support design enables higher synthesis scales, steadier pressures, and lower solvent use while preserving yield and purity across diverse oligonucleotide lengths.

  5. Commercially Proven Sterile Fill/Finish With Capacity And Global Backing 1/27/2026

    Find comprehensive solution with new sterile fill/finish investments supporting complex molecules through robust tech transfer, commercialization expertise, and integrated cGMP manufacturing solutions.

  6. Lyo‑Modelling For Risk Reduction And Process Insights 1/26/2026

    Use lyophilization modelling to optimize freeze‑drying, boost product quality, and lower commercialization risks through predictive insights, robustness analysis, and deeper process understanding.

  7. Handle Your Large-Scale Buffer Preparation Efficiently 1/23/2026

    Discover how to prepare 10x PBS using an innovative system to ensure scalable, efficient, and consistent buffer preparation for large-scale workflows.

  8. Manufacturing ADCs: Extractables In Single-Use Systems 1/23/2026

    Antibody-drug conjugates offer targeted cancer treatment with reduced toxicity. Discover how single-use technologies simplify ADC manufacturing to ensure safety, flexibility, and efficiency.

  9. Measure And Control In-Line Protein Concentration 1/22/2026

    Streamline protein and antibody purification with an automated TFF system featuring real-time, in-line concentration measurement for enhanced accuracy, reliability, and cGMP compliance.

  10. Tailored, Cutting-Edge Lyophilization For Biologic Stability 1/21/2026

    Advanced lyophilization uses quality‑by‑design, predictive modeling, and tailored processes to boost biologic stability, reduce cold‑chain needs, and enable scalability for complex therapies.