PHARMACEUTICAL ONLINE RECENT WEBINARS
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.
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.
Curing The Cost Of Poor Quality: How Argon Medical Found The Remedy
Discover how poor quality can cost your organization up to 20% of its revenue and learn how Argon Medical's eQMS helped them reduce defects, waste, and complaints.
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.
Minimizing Risk In RNA-LNP Encapsulation And Drug Product Manufacturing
Learn about an integrated drug substance/drug product offering for your IND program and beyond, with a holistic approach to ensure process robustness at every stage.
Embracing Today, Shaping Tomorrow: 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.
Adapting To Evolving Regulations: Validation In A Changing Landscape
Discover how evolving regulatory expectations in life sciences present new challenges and opportunities, as well as gain insight into strategies from experts in the field to navigate risk-based validation processes.
Do Not Bear Cross Contamination In The Pharmaceutical Industry – Prevent It
Learn how thorough cleaning and process optimization in pharma manufacturing prevent cross-contamination, ensure product integrity, and enhance efficiency while also improving compliance and reducing costs.
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.
Rapid Delivery Of Toxicological Study Material: Accelerating Development
Explore key strategies and technologies designed to address the analytical considerations and material flows to facilitate the rapid delivery of toxicological material.
How High Drug Load Nanocrystalline Tablets Lower Pill Burden
We showcase the development of high drug load nanocrystal based tablets and prove that nanocrystals can match the pharmacokinetic performance of ASDs while reducing the overall pill burden.
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.
Get $mart: 1 Year Out From Phase 1 Injectable Trials, Avoid 3 Expensive Mistakes
Learn how to scale up injectable drug production for Phase 1 trials, avoid costly mistakes, and find the right CDMO partner for long-term success.
Bioprocess Optimization: Leveraging Functional DOE With Time-Based Insights
Explore the key differences between traditional DOE and Functional DOE as Seongjin Kim demonstrates how the latter enhances bioprocess optimization through a fed-batch cell culture example.
Digital Enhancements For Operational Excellence
Unlock operational excellence with digital enhancements. Discover practical strategies to reduce errors, streamline processes, and drive continuous improvement across industries.
De-Risking Early Phase Micronization With Integrated Solid Form Selection
Review a case study describing the selection of the optimal solid form of an API designed for pulmonary administration through the pulmonary route.
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.
Contract Manufacturing: Must-Know Trends And Strategies For 2025
Regulated industries face rising demand, tech breakthroughs, and regulatory harmonization. Discover how contract manufacturers must leverage AI and cloud solutions to stay agile and compliant in the future.
Essential Considerations For Selecting The Right Biologic Fill/Finish Partner
Partnering with a provider that prioritizes quality and yield optimization not only ensures product safety but also helps reduce operational costs.
CMC And Clinical Strategies For Developing Injectable, Oral Peptide Drugs
In this session, Chief Scientific Officer Dr. Andy Lewis delves into the key drivers shaping peptide drug development and explores innovative delivery options to enhance therapeutic outcomes.
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.
Accelerating Clinical Development: Modern Tools In Process Chemistry
Whether you aim to address bottlenecks or explore advanced techniques, gain a practical and forward-thinking perspective to streamline early-phase development with HTE and model-based approaches.
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.
Demystifying Large Scale Continuous Chromatography For Small Molecules
Learn the fundamentals of developing a continuous chromatography process with Simulated Moving Bed (SMB) technology for small molecules, from gram-scale to multi-ton commercial production.
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.
Project Delivery Methodology To Accelerate Operational Readiness
Learn how to implement a focused operational readiness model that goes beyond traditional construction and startup schedules. Discover how this approach can reduce timelines and improve project success.
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.