On demand webinars in analytical and bioanalysis
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WebinarRisks of non-compliance: managing impurity control and challenges with reference materials
USP explored the latest approaches to organic impurity analysis and scientific solutions to support pharmaceutical quality, including regulatory expectations and practical applications of the USP Reference Standards.
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WebinarEnsuring drug quality: mastering stability testing in pharma
Watch this webinar to discover how UV-Vis spectroscopy and gas chromatography support API monitoring, testing and analysis.
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WebinarRegulatory shifts ahead: preparing for EU pharmaceutical reform and FDA changes
With the EU’s pharmaceutical legislation reform soon to come into force, regulatory experts outline what is changing across both US and European frameworks and how sponsors can position pipelines ahead of implementation.
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WebinarOptimising efficiency and yield through bioprocessing automation
Watch this webinar to explore how process Raman spectroscopy supports bioprocessing automation across upstream and downstream workflows, helping teams increase yields, improve process efficiency, and ensure more consistent product quality.
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WebinarPractical steps for innovating pharmaceutical manufacturing
In this webinar, industry experts discussed practical examples and considerations for transforming manufacturing processes.
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WebinarSmarter Raman QC for biopharma fill-finish with scalable model transfer
Join this webinar to explore how modern Raman spectroscopy is transforming biopharma fill-finish quality control through faster analysis, multi-attribute insight, and scalable model transfer.
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WebinarThe either-or trap: consequences of enhanced mechanical calibration vs fully qualifying your dissolution equipment
USP expert discusses how to confidently qualify your dissolution equipment and avoid costly testing errors.
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WebinarThe future of contamination control in pharma: from compliance to innovation
This webinar explores the benefits of accelerated microbial identification using MALDI-TOF in pharmaceutical contamination control strategies.
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WebinarRisks in pharmaceutical quality - the role of reference standards in analytical procedures
Join this webinar to learn about the essential role of Reference Standards in mitigating risks to pharmaceutical quality.
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WebinarControlling impurities in pharmaceutical waters
This virtual panel explores impurity control in pharmaceutical waters, the differences between microbial and organic contaminants, and best practices for measurement and treatment.
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WebinarEnhancing manufacturing with process analytical technology (PAT) in 2025
During this virtual panel, industry experts will explore the latest developments and biggest challenges in process analytical technology (PAT) today.
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WebinarHow a well-orchestrated digital ecosystem drives laboratory efficiency and innovations
Find out how to take advantage of a connected digital ecosystem to enhance quality control, streamline manufacturing and, ensure regulatory compliance
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WebinarBenchtop NMR for continuous process monitoring in PAT
Discover how Bruker Benchtop NMR integrates with synTQ software, enhancing process monitoring and complementing IR and Raman techniques in the PAT framework
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WebinarWhen innovative formulations cloud sterility testing
Webinar presented by Miriam Guest, Senior Principal Scientific Advisor at Charles River, to explore how ATP-bioluminescence outperforms traditional sterility testing in complex matrices.
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WebinarUnmasking the unknown: how mass spectrometry delivers accurate identifications
In this webinar, learn more about advanced techniques like mass spectrometry which can help identify unexpected impurities in drug substances and drug products.
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WebinarDefining the right digital strategy for oncology: What do you want to measure?
In this webinar, find out how to optimise oncology clinical trials using digital tools to accelerate decision-making.
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WebinarManaging the complexities of NDSRI method development: The N-nitroso propranolol case story
In this webinar, Dr Marian Twohig, Principal Scientist at Waters Corporation, will provide an overview of the more recent progress around N-nitrosamine regulations.
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WebinarPharmaceutical continuous manufacturing: what’s next for industry?
During this virtual panel, industry experts will discuss adoption of continuous manufacturing in the pharmaceutical industry.
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Enhancing biopharma workflows with the power of UV/Vis spectroscopy
Discover the valuable role ultraviolet-visible spectroscopy can play in quickly and accurately monitoring a drug as it moves through the research & development workflow and enabling quality and regulatory compliance through the manufacturing process.
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Webinar
Process analytical technology: applications and opportunities for pharma
During this virtual panel, industry experts will discuss the latest advances and applications of process analytical technology in the pharmaceutical sector.