Webinars
Exclusive free live webinars for the pharmaceutical industry. Catch-up on pharmaceutical webinars you may have missed with our video on demand archive.
Upcoming webinars
Webinar
Ensuring drug quality: mastering stability testing in pharma
Join this webinar to discover how UV-Vis spectroscopy and gas chromatography support API monitoring, testing and analysis.
More upcoming webinars
Modernising pharma QA/QC laboratories: preparing for a more connected, compliant future
Join this webinar to discover how modern QA/QC laboratories are embracing digital transformation to enhance compliance, workflows and data integrity to build a more connected, future-ready pharmaceutical quality ecosystem.
From passive to active air monitoring in aseptic filling: a risk-based approach to replacing settle plates
In this webinar, Particle Measuring Systems will share a case study of a biopharmaceutical company developing and applying a structured global rationale for the implementation of continuous viable environmental monitoring with a single-use microbial impactor within aseptic manufacturing environments.
The impact of negative control stability on recombinant endotoxin testing
In this webinar, FUJIFILM Wako Chemicals Europe GmbH will present the results of a study evaluating how NC stability in endotoxin detection reagents affects assay performance.
Building quality and consistency into accelerated cell and gene therapy development
How can cell and gene therapy manufacturers move programmes forward faster without compromising quality, scalability or regulatory readiness?
Editor's Picks
WebinarThe impact of negative control stability on recombinant endotoxin testing
In this webinar, FUJIFILM Wako Chemicals Europe GmbH will present the results of a study evaluating how NC stability in endotoxin detection reagents affects assay performance.
WebinarBuilding quality and consistency into accelerated cell and gene therapy development
How can cell and gene therapy manufacturers move programmes forward faster without compromising quality, scalability or regulatory readiness?
WebinarFrom passive to active air monitoring in aseptic filling: a risk-based approach to replacing settle plates
In this webinar, Particle Measuring Systems will share a case study of a biopharmaceutical company developing and applying a structured global rationale for the implementation of continuous viable environmental monitoring with a single-use microbial impactor within aseptic manufacturing environments.
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On Demand Webinars
Catch-up with our free video on demand webinars
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.
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.
WebinarImplementing reporter assay-based MAT for rapid pyrogen detection
Watch this webinar to discover how reporter assay-based MAT can help laboratories accelerate pyrogen testing, simplify workflows and support the transition to animal-free testing while maintaining confidence in results.
WebinarChoosing the right crystal: solid form optimisation for pharmaceutical development
Hear from Dr Zi Li, Associate Director of Formulation at BioDuro, to explore how polymorph screening, salt formation and cocrystallisation can resolve dissolution, stability and IP challenges in early-stage drug development.
WebinarEnhancing Laboratory Workflows with qPCR Automation
In this webinar you will learn how automation can support scale throughput while maintaining data quality and reproducibility in PCR and qPCR workflows.
WebinarHow thermal analysis can enhance pharmaceutical drug development
This webinar discussed three core techniques to optimise drug development through assessment of a material’s stability, composition, impurities, humidity effects, and thermal properties.
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.
WebinarHarnessing digital PCR for rapid sterility testing
Explore rapid sterility testing methods that ensure fast, reliable product release, addressing critical challenges in timely delivery and safety.
WebinarPractical steps for innovating pharmaceutical manufacturing
In this webinar, industry experts discussed practical examples and considerations for transforming manufacturing processes.
WebinarPractical considerations for aseptic gowning in contamination control strategies
Watch this webinar as we examine the main personnel-related factors that could lead to particle/microbial contamination risks of the product and outline practical measures that can mitigate these risks.
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.
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.
WebinarHarnessing AI for more efficient clinical trials
During this virtual panel, industry experts discussed practical examples and considerations for applying AI in pharma’s clinical trials.
WebinarIncreasing the effectiveness of pharma endotoxin testing
During this virtual panel, industry experts will discuss the evolution of endotoxin testing, future trends and key risk mitigation considerations for pharma companies.
WebinarRealising autonomous pharmaceutical operations
Is operational complexity limiting your performance? Discover how autonomous technologies are reducing risk and improving quality in pharma organisations.
WebinarAutomating quality control testing for radiopharmaceutical production
This webinar showcased a rapid microbial method that can help to address the time to result challenge posed by short shelf-life radiopharmaceuticals.
WebinarThe future of sterility testing: one-day results with advanced RT-rt PCR technology
Watch this webinar to find out how RT-rt PCR is revolutionising sterility testing and discover a unique approach that provides reliable one-day results and enhanced sensitivity and detection capabilities.
WebinarMastering impurity profiling: USP’s evolving standards and strategies
Watch our webinar with USP as they explored new approaches for impurity profiling - unveiling new frameworks, analytical tools, and regulatory insights that are reshaping pharmaceutical quality standards.
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.
WebinarBest practices for PUPSIT assembly design and operation
This webinar explores the design and implementation of pre use post sterilisation integrity test assemblies (PUPSIT) in sterile filtration processes to ensure regulatory compliance while minimising operational risk.
WebinarHarnessing AI to transform quality and manufacturing in life sciences
This webinar explores innovative, purpose-built AI solutions that elevate compliance and efficiency in quality and manufacturing operations.
WebinarLipid formulations in softgels - enhancing bioavailability and therapeutic efficacy
This webinar will explore how lipid formulations in softgels can enhance drug absorption and bioavailability.
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.
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.