On Demand Webinars
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.
Maximizing value across drug development: Embracing a new CDMO and CRO partnership approach
Pharma and biotech companies are facing increased competition and rising costs, alongside the ongoing pressure to deliver innovative therapies faster than ever.
Waters Bioprocess Walk-Up Solutions
Learn how to improve process understanding and robustness, reduce costs and automate routine product quality and cell culture media analyses with a streamlined interface for sample preparation and LC-MS analytics. Real-time data acquisition and processing for informed decision-making.
Mastering analytical methods for fail-safe PPQ
After investing significant financial and temporal resources in the development of a new biologic molecule, companies cannot afford any setbacks in the final stages.
Pitfalls of PPQ: top risks and how to mitigate them to ensure successful commercialization
You’re almost at the finish line and you need to prove your biologic therapy's production process is robust and consistently meets purity, quality, and potency standards.
