PHARMACEUTICAL ONLINE RECENT WEBINARS
How To Address Your Solid Dosage Processing Needs
Unlock the keys to consistent solid dosage products. Learn to align unique product needs with optimal processing requirements and equipment strategies. Gain a roadmap for improved quality and reproducibility.
Smarter CMC Strategies To Accelerate Next-Gen Biologics To The Clinic
Learn how process design and cross-functional collaboration mitigate risks and accelerate the path from early development to FIH manufacturing through real-world case studies of practical approaches.
AI In Action: Driving Operational Excellence In Life Sciences
Discover how combining domain expertise with advanced AI and data engineering automates compliance, accelerates readiness, and provides real-time insights for confident decision-making.
Integrated Manufacturing To Mitigate CMC Risks, Simplify Commercial Supply
Leveraging cross-functional coordination between sites, harmonized tech transfers, one quality system, and synchronized team activities can streamline regulatory submissions and deliver high-quality commercial outcomes.
Driving Operator Safety And Process Efficiency
Discover how ergonomic design and workflow simplification can turn routine production tasks into strategic advantages, as well as practical ways to boost safety, efficiency, and innovation.
From First-In-Human To Proof-Of-Concept — Quicker, Smarter, Streamlined
Explore examples of smarter SAD/MAD trial designs including multi-part and hybrid protocols, regulatory foresight, recruitment considerations, and operational strategies that keep programs moving.
Evolving Gene Editing For Rare Disease Drug Development
Explore how scalable gene editing platforms are advancing therapies for ultra-orphan conditions, with insights into manufacturing models, regulatory strategies, and clinical approaches.
Compliance To Confidence: Annex 1 For Small-Batch, High-Value Production
Get strategies for meeting the updated GMP Annex 1 in small-batch aseptic filling. Learn about contamination control, quality management, and equipment design for high-value liquid and powder products.
Liquid Phase Peptide Synthesis: Regulatory, Analytical, And QC Perspectives
Discover how Liquid Phase Peptide Synthesis (LPPS) uses traditional reactors to create more efficient and sustainable peptide manufacturing. Learn about key analytical and quality control considerations.
Supply Resiliency For Bioprocessing Amid Global Volatility
Build bioprocessing resiliency with strategic supply chain management. Learn to meet quality, compliance, and time-to-market demands amid global volatility with effective sourcing.
Process Intensification Strategies For Smarter Biomanufacturing
Explore how biopharma leaders are using process intensification to modernize facilities, cut costs, and increase yield with practical strategies and real-world case studies.
Optimizing Aseptic Processing With Isolator Technology
Discover how pharmaceutical isolators optimize operations, achieve higher sterility assurance, and meet stringent regulatory requirements. Learn about design principles, validation, and VHP cycles.
Filtration Unfiltered: Technology To Meet New Bioprocessing Challenges
Explore how filtration strategies are adapting to diverse molecule pipelines, regulations, and sustainability targets with insights into process intensification and the technologies shaping the future.
How Digital Cleaning Validation Can Simplify Audit Readiness And Improve Compliance
Discover how to enhance audit readiness and improve compliance by shifting to a digital cleaning validation program. Learn to determine worst-case products and maximum safe carryover limits.
Future Of Pharma Packaging: Trends, Tech, And Patient Solutions
Explore how traditional and innovative pharmaceutical packaging formats improve patient adherence, support emerging therapies, and shape the future of drug delivery and treatment outcomes.
Not All Manufacturing Automation Is Created Equal
Learn how outcome-based automation helps life sciences manufacturers reduce risk, improve performance, and drive measurable results—by aligning tools with business goals.
Streamlining Biologics Development: Leveraging Small-Scale Studies For Greater Efficiency
Uncover how a data-driven approach to small-scale studies not only accelerates development timelines but also enhances decision-making and resolves full-scale manufacturing challenges across diverse biologic modalities.
Assessing Production And Stability Of Antibody Drug Conjugate Platforms
ADCs with similar antibody sequences can behave differently due to linker and payload choices. Analytical tools reveal structural and stability differences critical to therapeutic performance.
Scientific Insights Into VHP Biodecontamination And BI Quality Management
VHP biodecontamination ensures aseptic manufacturing, but BI variability challenges validation. Addressing rogue BIs and regulatory shifts strengthens contamination control and process reliability.
Streamlining Vaccine Purification: Techniques For Modern Modalities
Explore cutting-edge chromatography techniques accelerating vaccine purification across diverse modalities, with case studies on HPV, Malaria, and COVID-19.
Innovation And Efficiency - Visual Inspection In The 21st Century
Digitizing your visual inspection processes is key to unlocking efficiency and ensuring compliance with global regulatory standards. Learn how to transition from paper-based systems to a digital database.
Using Innovation To Accelerate And Optimize Your Scale-Up Strategy
Explore how AI, QbD, and digital transformation are reshaping manufacturing to accelerate scale-up, reduce defects, and optimize batch release for faster, more resilient operations.
Nanoforming Biologics, GLP-1s: From I.V. To Sub Q And Inhaled Delivery
Developing new delivery routes is essential for creating more effective treatments. Nanoforming enables new routes to simplify dosing, enhance patient comfort, and reduce healthcare costs.
Benefits Of Outsourcing To An Integrated CDMO
Streamlining ADC development through an integrated CDMO can reduce risk and improve quality. Discover why specialized expertise in linker chemistry and bioconjugation is key to overcoming the complexity of ADC manufacturing.
Strategic Approaches To Controlled Release Formulation: Polymer Screening And Case Study Insights
Discover how early polymer selection drives formulation success, with case studies linking polymer choice to drug release and practical insights for developing robust CR products.
Cell Cycle Mapping In Tumors With Advanced Technologies
Discover how spatial profiling and advanced imaging tools are transforming drug discovery, featuring Wayne Stallaert’s lab’s work on cell cycle mapping and biomarker insights in cancer research.
Building Quality By Design For Multi-Specific Therapeutic Proteins
Platforms incorporating high throughput in silico screening, in vitro expression, and immunosafety of multi-specific molecules can help mitigate potential developability risks and accelerate timelines.
Scaling Plasmid DNA Production: A Proven Strategy For Higher Yields
Learn how an agile manufacturing partner scaled their plasmid DNA production and achieved higher yields by optimizing their media selection and fermentation processes.
Next-Gen Disease Models And Cell Therapeutics: Innovations In AI, Omics And Collaboration
Learn how to leverage AI, omics integration, and collaborative research to build more physiologically relevant disease models and accelerate the development of next-gen cell therapies.
Efficient Scale-Up Of Monoclonal Antibody Production: From Bench Top To 500L
Scaling monoclonal antibody production from the lab to a commercial scale can be challenging. Learn about an approach that helps you maintain consistent productivity and product quality across all scales.