Webinars
Latest Webinars
- Previous
- Next
Featured Webinars
Webinar
How thermal analysis can enhance pharmaceutical drug development
This webinar will discuss three core techniques to optimise drug development through assessment of a material’s stability, composition, impurities, humidity effects, and thermal properties.
WebinarPractical steps for innovating pharmaceutical manufacturing
During this virtual panel, industry experts will discuss practical examples and considerations for transforming manufacturing processes.
Editor's Picks
WebinarThe either-or trap: consequences of enhanced mechanical calibration vs fully qualifying your dissolution equipment
Register for this exclusive USP webinar
WebinarHow thermal analysis can enhance pharmaceutical drug development
This webinar will discuss three core techniques to optimise drug development through assessment of a material’s stability, composition, impurities, humidity effects, and thermal properties.
- Webinar
Practical steps for innovating pharmaceutical manufacturing
During this virtual panel, industry experts will discuss practical examples and considerations for transforming manufacturing processes.
Join now
Unlock exclusive industry insights
- Bookmark articles and resources to access anytime
- Enjoy free access to industry leading resources, webinars and insights
- Stay informed with the latest news and breakthroughs in drug discovery
- Receive updates and recommendations tailored to your research interests
Recent Webinars
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.
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.
WebinarAchieving rapid microbial method validation with precise reference standard quantification
This webinar explores validation of rapid microbial methods with ready-to-use reference materials, a new industry standard in microbial QC testing.
WebinarReflections and future opportunities in pharmaceutical microbiology
During this virtual panel, industry experts will explore the major challenges, promising innovations and key trends impacting pharmaceutical microbiology. Watch on demand now.
WebinarWhat does the future hold for drug formulation in 2026?
During this virtual panel, industry experts will explore the latest innovations and major challenges of drug formulation in the pharmaceutical industry.
WebinarLeveraging early insights to accelerate the oral drug development cycle
This webinar explores oral drug product development and how to address critical challenges such as complex formulations and regulatory hurdles.
WebinarSafety reporting in clinical trials: six core considerations for success
This webinar will provide guidance in navigating the terrain of pharmacovigilance, including regulatory challenges, and gain a deeper understanding of the pivotal role played by safety reporting in clinical research.
WebinarFast tracking clinical success: choosing the right Fill & Finish CDMO
Selecting the right Fill & Finish CDMO can make or break a product’s commercial success. In this webinar, join industry experts to explore key strategies for navigating this crucial stage, ensuring optimal efficiency where it matters most.
WebinarOptimizing micronization and spray-drying to achieve high yields from clinical to commercial
Gain expert insight into optimizing pharmaceutical particle engineering while maintaining product quality and optimizing yield, from formulation through commercial supply
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.
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
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
WebinarTrends for life sciences quality leaders in 2025 - mastering what matters
This webinar explores the major trends impacting life sciences in 2025 and how the pharma industry can capitalise on the latest developments shaping quality management.
WebinarNavigating pharmaceutical environmental monitoring in a changing industry
During this virtual panel, industry experts explore the latest advances in environmental monitoring, discuss key challenges within the sector and approaches that can prevent and mitigate these issues.
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.
WebinarThe path to optimisation in pharmaceutical microbiology
During this virtual panel, industry experts will delve into the latest advances and biggest challenges in pharmaceutical microbiology today.
WebinarTurning quality management into quality leadership
This webinar discusses the power of a comprehensive QMS to ensure efficiency, compliance, and product quality.
WebinarMonocyte activation test (MAT): Insight into examining regulations and markets prospects
Watch this webinar to learn about the current regulations on the monocyte activation test (MAT) and the new type of MAT entering the markets.
WebinarAn alternative medium to support sterility testing using the Growth Direct® Rapid Sterility System
Watch on demand to learn how a new single medium, Rapid Sterility Medium (RSM), performs as well as or better for the growth promotion of test microorganisms compared to compendial sterility test media.