Harnessing Potential: Innovations And Improvements In Viral Gene Therapy

Review the potential of AAV-mediated gene therapy as a platform approach to treat multiple genetic neurological diseases, and explore suggestions to streamline translational studies and reduce costs.

Inside The Development Of An AAV8 Production Platform

Explore innovative solutions for AAV8 production challenges, which include scalability and purity, as well as learn how a collaboration with CDMO Matica Biotechnology ensures efficient, high-yield gene therapy vector production.

Sustainable Manufacturing Through Efficient BioProduction Unit Operations

Accelerating Clinical Data Review With Traceable Workflows

Discover how streamlined workflows and enhanced collaboration between data managers and medical reviewers can boost clinical trial efficiency, improve data quality, and ensure patient safety.

Sterile Gas Filtration And Optimization In Bioprocessing

Unlock insights into sterile gas filtration challenges in bioprocessing. Watch this on-demand session to learn optimization strategies for critical applications and improved filter performance.

Navigating Global Regulatory Landscapes In An Evolving Biopharma Industry

Minimize regulatory risks and ensure compliance in the evolving biopharma sector. Watch this on-demand discussion for insights on change management, supplier collaboration, and future market trends.

Transforming Rare Disease Drug Development For A Faster Cure

This comprehensive exploration aims to shed light on the critical aspects of expediting curative therapies, with a focus on the strategic role that CDMOs can play in this transformative journey.

Optimize Your Process For Producing High-Concentration Drugs

Explore the challenges and solutions in high-concentration monoclonal antibody manufacturing, which includes practical strategies for maximizing product recovery and optimizing processes for efficient production.

Development Strategies For Platform Devices Navigating Regulatory Complexities

Explore regulatory strategies for platform drug-device products, including bridging formulations, leveraging existing data, and aligning with FDA expectations to accelerate market access and reduce risk.

Critical Imaging Risks In GLP-1 And Neurology Studies

In the evolving landscape of GLP-1 and neurology clinical trials, imaging has become a pivotal tool for evaluating both efficacy and safety. Delve into the early indicators of imaging-related challenges and insights into preclinical strategies for effective risk mitigatio...

Optimal Tech For Predicting Drug Responses At The Cellular Level

Explore how preserving spatial molecular information and leveraging AI-driven spatial-omics can transform treatment prediction, patient stratification, and personalized medicine.

Driving Innovation In Decentralized Manufacturing

Unlock the potential of localized manufacturing and see how cutting-edge technology is transforming access to essential medications, ensuring patients get what they need.

Clinical-Grade Manufacturing Of Difficult-To-Transduce Cells

Discover how Miltenyi R&D and Bioindustry experts revolutionize cellular therapy with BaEV-env LVVs as well as gain insights into preclinical evaluations and clinical-grade product development for CAR-NK cells.

Tools For Efficient Downstream Processing Of Antibody-Based Therapeutics

Watch and discover how to effectively utilize chromatography tools for improved purification of therapeutic monoclonal antibodies and antibody derivatives.

Who's In Charge? How To Ensure Effective Trial Oversight, Leadership

Gain valuable insights into the role of sponsor-side Clinical Operations leadership, the risks of over-relying on CROs, and key strategies for fostering collaboration between sponsors and partners.

Human Factors Testing: Engaging End-Users In Med Device Development

Explore the significance of human factors in the development of medical devices through an illustration of how important it is to incorporate the end users in the device development process.

Discovery Through Commercialization: A Biologic Drug's Analytical Journey

Gain valuable insights into advanced methods and analysis techniques for high-order structure, physiochemical characterization, cell-based and biochemical assays, and more.

From Research To Reality: Overcoming CMC Challenges In Cell & Gene Therapy

Explore the importance of adopting a Quality by Design (QbD) approach in the development process while integrating regulatory and CMC strategies for maximum efficiency and benefit.

Efficient Downstream Processing Of Antibody-Based Therapeutics – A CDMO Perspective

Discover efficient downstream processing strategies for antibody-based therapeutics. Explore key considerations and trade-offs in purity, yield, speed, and cost, from a CDMO perspective.

The Next Frontier In mRNA: Modular Manufacturing For Scalable RNA-LNP Therapies

Explore constructing a modular RNA-LNP GMP facility using Cytiva's FlexFactory™ process train in a KUBio™ environment to scale RNA-LNP therapies.

Quality Roundtable: Raw Material Planning For Tech Transfer And Scaling Biologics

Join this roundtable of biopharmaceutical professionals as they share their insights to help you navigate important quality and planning decisions for the progression of your biologic.

Quantifying And Assessing Cleaning And Disinfection Residues: A Case Study

Ensure your ATMP facility meets the latest Annex 1 standards for cleaning & disinfection residue control with the help of practical guidance and a case study detailed in this presentation.

Rapid Process Development And Technical Support For AAV Scaleup

Accelerate your AAV production journey. Learn how rapid process development and expert support can streamline your path from vial to purified bulk, ensuring scalable and efficient manufacturing.

mAb Up- And Downstream Process Intensification Strategies

Discover how to reduce monoclonal antibody (mAb) manufacturing time and costs through process intensification. Learn about continuous perfusion, ultrahigh cell density banks, and more.

Uncovering The Root Cause Of Clinical Trial Troubles

Discover essential strategies to prevent clinical trials from reaching a crisis while gaining a deeper understanding of the importance of addressing systemic issues early.

Innovative AI Software Solutions Driving Biomarker Research Efficiency

Join our webinar to explore how Genedata Profiler and Leica Aivia AI-powered tools streamline biomarker discovery, enhance data analysis, and improve research efficiency in personalized medicine.

Leveraging Platform Processes For Developing And Accelerating Novel Gene And Cancer Therapeutics

Explore how platform processes advance gene therapies, the impact of strong partnerships on patient access, and the future shaped by these collaborations.

Navigating Primary Packaging Challenges, Solutions For Emerging Innovators

If you are in the process of developing a complex or sensitive injectable drug, learn about containment solutions to mitigate your risks and help you get your drug to the patient faster.

How To Boost AAV Titer With Feed Supplementation In Both HEK293 And Sf-9 Platforms

Explore how optimizing post-transfection or post-infection feeding in HEK293 and Sf-9 cells significantly boosts AAV titers, enhancing production efficiency for gene therapy applications.

Using An Adherent Platform To Scale-Up An Upstream Viral Vector Process

Gain insight into a helper-dependent adenovirus (HDAd) process that covers everything from bench-scale and optimization to tech transfer.