On-Demand Downstream Manufacturing Webinars

1. Using Residual DNA Quantification Data To De-Risk mAb Development 6/11/2026

   Residual DNA quantitation offers more than impurity measurement. When used across process steps, it helps compare purification performance, identify risks early, and ensure assays remain reliable.

2. Efficient mAb Development With A Flexible Purification Toolkit 6/4/2026

   Increasing mAb complexity is pushing purification beyond traditional platforms. See how flexible chromatography, optimized buffers, and adaptable workflows are becoming essential to achieve target purity.

3. How Solid-State Science Solves Your Toughest API Challenges 6/3/2026

   Difficult small molecules demand more than standard purification strategies. See how combining solid-state expertise with advanced chromatographic modeling improves filtration, purity, and scalability.

4. Process Development And Intensification For UF/DF Of Viral Vectors 6/3/2026

   Optimizing TFF in viral vector workflows can reduce processing time while improving yield. Comparing TMP and permeate control strategies highlights key trade-offs to guide your purification decisions.

5. mAb Aggregate Control On-Demand Webinar 5/22/2026

   Aggregation can undermine yield and quality in downstream mAb processing. Learn practical capture, polishing, and TFF strategies to prevent and reduce aggregates, with a focus on chromatography.

6. Scalable Purification Strategies For Antibody-Drug Conjugates 5/21/2026

   Mixed mode chromatography offers a targeted way to control ADC aggregates and DAR profiles. Learn how tuning key parameters and leveraging hydroxyapatite polishing can improve selectivity, scalability, and batch consistency in downstream purification.

7. Design Scalable Downstream Processes With Practical Strategies 5/11/2026

   Downstream purification is becoming more complex as new modalities enter development. Learn how advanced analytics and chromatography strategies can support scalable, confident process development.

8. 3 Critical UF/DF Challenges And How To Solve Them 5/4/2026

   High‑concentration mAbs change how UF/DF behaves. Learn how modern TFF platforms help address these challenges and maintain control as formulations move beyond traditional limits.

9. A Gentler Workflow: Fc-fusion Protein Purification With Mixed-Mode And Anion Exchange Chromatography 3/26/2026

   Gain insights into comparative performance, workflow flexibility, and practical considerations for implementing a new weak anion exchange hydrophobic resin and a strong anion exchange resin.

10. Ensure Successful Viral Clearance 3/26/2026

    A decade of viral clearance data comparing established and emerging operations, highlighting LRV performance, key process risks, and practical insights to strengthen downstream safety.