Quality Risk Management tools to improve data integrity in micro QC
ON-DEMAND By Charles River Laboratories
Watch this on-demand webinar with Jordi Iglesias to learn how you can improve the data integrity of your microbiological QC assays.
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Webinars
Emerging tools for the analysis of biologics and biosimilars
ON-DEMAND By Bruker Biospin Group
In this virtual roundtable, experts explore the uses of nuclear magnetic resonance (NMR) in the analysis of biologics and biosimilars and discuss how recent advances are changing the game.
How data integrity is your first step toward a Pharma 4.0 strategy
ON-DEMAND By Thermo Fisher Scientific
Watch this webinar on demand to learn how a complete, integrated laboratory software system provides streamlined processes and drives data integrity, advancing organisations toward a Pharma 4.0 strategy.
A holistic strategy to ensure container closure integrity of sterile vials
ON-DEMAND By Lighthouse Instruments
Watch our on-demand webinar where we describe a more science-based holistic approach to ensure CCI; a framework that includes robust design and qualification of the process and the implementation of appropriate process controls is required.
Data integrity and digital workflow guidance in a contemporary pharma lab
ON-DEMAND By Sartorius
During this on-demand webinar we discuss how to achieve data integrity and give real examples from the US Food and Drug Administration (FDA) warning letters about the most frequent and typical violations.
Implementing Pharma 4.0 on water systems – FAQ for increasing efficiency with TOC and conductivity
ON-DEMAND By SUEZ – Water Technologies & Solutions
In this on-demand webinar you will learn from two experts with deep expertise in online monitoring, UPW, RTT, TOC, conductivity, cleaning validation and Pharma 4.0.
Comparing EMA and Health Canada CTA submission for Phase I trials to US FDA IND application
ON-DEMAND By Altasciences
Watch this webinar on-demand which presents an overview of a foreign health authority’s requirements for gaining approval to conduct an FIH clinical trial by comparing Health Canada and European Medicines Agency (EMA) Clinical Trial Authorisation (CTA) processes to that of the FDA IND submission.
Unique advantages of incorporating untargeted and targeted metabolomics in drug development and clinical trials
ON-DEMAND By Metabolon
Watch our on-demand webinar as experts discuss the use and benefits of incorporating untargeted and targeted metabolomics into the drug development process.
Uncover the potential of your lab – discover how digital transformation can be so much more than just insights
ON-DEMAND By IDBS
Join our virtual roundtable panel where we discuss best practices and experiences of digital transformation, as well as exploring how digital transformation can help accelerate decision making, optimise processes and remove operational inefficiencies.
How to master raw material ID testing in 2021
ON-DEMAND By Thermo Fisher Scientific
In this on-demand webinar we explore the evolving role of handheld and portable instruments to drive quality improvements and manufacturing success in 2021.
Pharmacopoeia changes – what to check for on UV/Vis spectrometers, and how.
ON-DEMAND By Mettler-Toledo GmbH and Hellma GmbH & Co. KG
Watch the on-demand webinar to learn about the important UV/Vis spectroscopy-relevant changes in both USP and Ph. Eur. taking a closer look at their impact and the solutions available to ensure compliance.
Liquid-filled hard capsules: A flexible tool for rapid access to the clinic with poorly soluble and/or highly potent compounds
ON-DEMAND By Lonza Pharma & Biotech
Watch our on-demand webinar to learn about liquid-filled hard capsule technology has a proven record for addressing complex active pharmaceutical ingredient (API) formulation challenges, including bioavailability enhancement.
Roadmap to compliance in environmental monitoring
ON-DEMAND By Merck KGaA
This on-demand webinar provides an overview of a holistic approach to achieve compliance with good manufacturing practice (GMP) requirements for environmental monitoring (EM) in aseptic manufacturing areas, such as ISO 5 cleanrooms in traditional setup, RABS or isolators.
Quantitative transmission Raman for content uniformity testing
ON-DEMAND By B&W Tek, A Metrohm Group Company
In this on-demand webinar, development groups will learn how analysis with quantitative transmission Raman aids in formulation development and process development, Register today to learn more!
The analytical reality of recombinant endotoxin technologies
ON-DEMAND By Charles River
In this webinar we discuss the results of our latest study where we evaluated the ruggedness, repeatability and specificity of commercially available rFC products, as well as our own recombinant product in development, against a large panel of endotoxins.
