The path forward — Altasciences’ approach to project management
ON-DEMAND By Altasciences
Discover the opportunities Altasciences' hybrid approach to project management can offer your drug development programme.
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Webinars
Simplifying oligonucleotide characterisation with Microchip CE-MS
ON-DEMAND By 908Devices
In this on-demand webinar, 908 Devices present a microfluidic capillary zone electrophoresis-based separation coupled with HRAM mass-spectrometry for rapid characterisation of oligos in positive ionisation mode.
Direct quantitative analysis of biological particles using the Coulter Principle
ON-DEMAND By Beckman Coulter Life Sciences
Learn how the Coulter Principle can precisely measure minute distributions of biological particles. This principle can be used to analyse cyanobacteria, E. coli bacteria, CHO cells, CAR T cells, yeast cells, algae cells, fat cells, plant cells and more.
Adopting technology in the quest for digital transformation
ON-DEMAND By MasterControl
Watch our on-demand webinar to discover how MasterControl Manufacturing Excellence™ augments and enhances worker performance as part of digital transformation.
Leveraging extended reality (XR) technology to drive laboratory productivity
ON-DEMAND By Thermo Fisher Scientific
Learn how SampleManager XR software and Microsoft HoloLens can support implementing a digital strategy and drive forward digital transformation.
Improve efficiency and return on investment by adopting molecular spectroscopy techniques in pharma manufacturing
ON-DEMAND By Thermo Fisher Scientific
In this on-demand webinar, discover the differences between FTIR, NIR and Raman spectroscopy, learn how spectroscopy is applied in quality control labs and hear how implementation of these techniques increased efficiency and minimised costs.
The role of small molecule NMR in medicinal chemistry
ON-DEMAND By Bruker Biospin Group
In this on-demand webinar, Kathleen Farley (Senior Principal Scientist, R&D, Pfizer Inc) describes how nuclear magnetic resonance (NMR) spectroscopy is integrated into the Pfizer drug discovery pipeline and how the technique is used.
Quality assurance and data integrity from an auditors’ viewpoint
ON-DEMAND By Thermo Fisher Scientific
In this on-demand webinar, you will hear directly from industry auditors as they discuss the current regulatory framework for good manufacturing practice (GMP), including data integrity, validation and qualification for computerised systems in regulated laboratories.
Navigating the transition from IVDD to IVDR
ON-DEMAND By Tecan
This on-demand webinar brings three leaders in the field together to discuss the new regulations, responsibilities across the whole supply chain, documentation, the notified body application process and key timelines.
Variable pathlength spectroscopy for dilution-free concentration measurement in GMP environments
ON-DEMAND By Repligen
Watch this on-demand webinar, where we reviewed VPT and how it can be used in various applications, from protein therapeutics to gene therapy.
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.
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.
