News
Smarter Raman QC for biopharma fill-finish with scalable model transfer
1+ mon, 2+ week ago (379+ words) Sponsored by Thermo Fisher Scientific 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. Raman spectroscopy offers real advantages for biopharma fill-finish QC " non-destructive measurement,…...
How thermal analysis can enhance pharmaceutical drug development
1+ week, 2+ day ago (274+ words) Sponsored by TA Instruments 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. Thermal analysis is an excellent tool to characterise pharmaceutical materials and obtain…...
Optimising efficiency and yield through bioprocessing automation
11+ hour, 24+ min ago (326+ words) Sponsored by Thermo Fisher Scientific Join this webinar to explore how process Raman spectroscopy can support bioprocessing automation across upstream and downstream workflows. Glucose feeding, media addition, harvest rate, and bleed decisions in perfusion all benefit from high-frequency measurement, but…...
Practical steps for innovating pharmaceutical manufacturing
11+ hour, 24+ min ago (174+ words) Join this virtual panel to explore how to: Be an early registrant, secure your spot now >> A panel of industry experts will be confirmed soon, register now to be the first to know who will be leading the discussion. Is…...
Mastering dissolution equipment qualifications: beyond mechanical calibration
1+ week, 5+ day ago (381+ words) Join this webinar to understand why mechanical calibration alone is not sufficient to fully qualify dissolution testing equipment " and learn from USP experts how the new dissolution performance verification standard reduces variability and compliance risk. See USP data that demonstrates…...
Increasing the effectiveness of pharma endotoxin testing
3+ mon, 3+ week ago (464+ words) During this virtual panel, industry experts discuss the evolution of endotoxin testing, future trends and key risk mitigation considerations for pharma companies. As lipopolysaccharides (LPS) found in the cell walls of Gram-negative bacteria like E. coli and Salmonella, endotoxins can have…...
Harnessing AI for more efficient clinical trials - European Pharmaceutical Review
2+ mon, 3+ week ago (494+ words) During this virtual panel, industry experts will discuss practical examples and considerations for applying AI in pharma's clinical trials. Late in 2025 the US Food and Drug Administration (FDA) qualified its first artificial intelligence (AI) tool for use in clinical trials,…...
Harnessing digital PCR for rapid sterility testing
2+ mon, 3+ week ago (562+ words) Join this webinar to explore rapid sterility testing methods that ensure fast, reliable product release, addressing critical challenges in timely delivery and safety. This webinar focuses on rapid sterility testing solutions essential for products with short shelf lives. Learn how…...
Why speed and flexibility matter now more than ever
5+ mon, 1+ week ago (232+ words) The balance between speed, scale, and compliance has never been more critical. As GLP-1s, biosimilars, and advanced therapies reshape global priorities, pharma leaders face a new question: how can manufacturing infrastructure evolve fast enough to keep pace? Why speed and…...
The Future of Sterility Testing: One-Day Results with Advanced RT-rt PCR Technology
6+ mon, 4+ week ago (554+ words) 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. In the pharmaceutical and biotechnology industries, sterility testing remains a critical…...