Cell and Gene Manufacturing and Logistics

  1. Knowledge Culture Basics — Gene Therapy Education Series: Lentiviral Vectors 6/9/2025

    In this session of our ongoing education series on lentiviral vectors, we delve further into principles of lentiviral transduction and challenges in suspension-based lentivirus production.

  2. Advances In Custom Medium Development The Multi-Omics Difference 6/9/2025

    Spent media analysis continues to be an essential part of many media development workflows. Newer techniques, however, using state-of-the-art analytical technology, are becoming more popular.

  3. Advances In Microbial Fermentation Knowledge Culture 6/9/2025

    Presented by three experts, this session examines real-world examples of how different approaches to media formulation and process conditions can influence outcomes.

  4. Exploring The Challenges Of Cell Dissociation In Vaccine Manufacturing 6/9/2025

    Vaccine manufacturing relies on efficient cell dissociation methods. Explore the challenges of traditional approaches like trypsin and the benefits of animal origin-free alternatives for improved workflows.

  5. Master The Course In Cell Culture 6/9/2025

    Learn how to navigate the complexities of mAb production with actionable strategies for quality-driven processes, supplier selection, and future-proofing your biologic manufacturing systems.

  6. Freedom Cell Line Development Kits 6/9/2025

    Achieve high-performance cell culture results with advanced tools that deliver consistent protein quality, stable clones, and accelerated timelines for commercial production. 

  7. 5 Key Considerations For Companies Outsourcing Process Development 6/9/2025

    Venture capital in biotech remains strong post-pandemic, especially in cell and gene therapies. Discover five key factors to help companies choose between in-house and outsourced process development strategies.

  8. Lyophilization To Enable Drug Products Containing Labile Molecules 6/6/2025

    Develop lyophilized formulations to overcome stability challenges and significantly extend the shelf life of sensitive therapeutic products.

  9. Bioanalytical Development And Testing For LNPs 6/6/2025

    Streamline gene therapy development by partnering with a centralized, GLP-compliant bioanalytical lab for comprehensive biodistribution studies using techniques like LC-MS/MS, RT-qPCR, and ELISA.

  10. Cleaning Process Capability: Understanding Populations, Samples, And Sample Size Requirements 6/6/2025

    This article examines the role of sample sizes in the determination of cleaning process capability or process performance in the manufacture of drugs/therapies and medical devices.