On Demand Webinars
Environmental Sustainability at Lonza Small Molecules - Wastewater Incineration Reduction
Sustainability is at the forefront of the way Lonza runs its business. Thanks to its Vision Zero initiative, it aspires to reduce emissions, water consumption and waste, as well as work without incidents.
How to Deal with the Complexity of Drugs in Clinical Development
Increasing complexity and tight timelines are putting more pressure on professionals involved in clinical drug development.
Bridging Genomics and Proteomics: Interrogation of Prospective and Archived Samples for Population- Scale Biomarker Discovery
Modern omics have redefined our understanding of biology and disease but scaling these insights to population-level studies demands innovation in automation, sensitivity, and data integration.
Decentralized Trials: The future is now
Decentralised trials are no longer a thing of the future. This session will focus on how COVID-19 pandemic presented an opportunity to re-envision clinical trials, a change that was long overdue.
How can LIMS deliver value to your Pharma Manufacturing Lab?
Please join our upcoming webinar focused on how laboratory information management system (LIMS) can deliver value and efficiency, and increase productivity, in your pharmaceutical manufacturing laboratory. Thermo Fisher Scientific SampleManager LIMS software can provide a complete, scalable solution that meets all your laboratory needs.
Modern Requirements for Laboratory Balances: A Global Pharmacopoeial Perspective
Regulatory requirements for laboratory balances used in pharmaceutical analysis have undergone significant updates across major pharmacopoeias over the last years — including the USP (United States Pharmacopeia, latest version 07/2025), Ph. Eur. (European Pharmacopoeia, 07/2021, currently under revision), JP (Japanese Pharmacopoeia, 06/2024), and ChP (Chinese Pharmacopoeia, 03/2025).
Federated Future: Back to the Science of Discovery
This Revvity webinar showcases how cutting-edge AI, machine learning, and integrated informatics platforms are transforming antibody discovery and developability assessment.
Breakthrough Insights for Complex Biologics: Discover the Power of CDMS
Charge Detection Mass Spectrometry Simplify your path to success for biotherapeutics by gaining unprecedented insights into the most complex and mega-sized new modalities, with direct mass measurement for individual ions.
Rapid delivery of toxicological study material: The new critical path for accelerating biopharmaceutical drug development
As timelines from DNA to IND continue to shorten, the need for faster toxicology material delivery has become increasingly important to start studies as early as possible and avoid delays in IND submissions.
Optimizing Pharmaceutical Transportation Management in Europe: Mitigating Supply Chain Risks
The rapid rise of advanced therapies demands seamless logistics and risk mitigation—especially in Europe, where clinical trials are surging. Ensuring shipment integrity, avoiding delays, and maintaining temperature control is critical.
