Resources

White paper
08 March 2018

With the rapid adoption of cloud computing, learn how Thermo Scientific™ Chromeleon™ CDS supports moving from a traditional on-premise setup to a cloud based deployment and associated benefits and challenges.

White paper
12 February 2018

21 CFR Part 11 requires Food and Drug Administration (FDA)-regulated industries, including medical device manufacturers, drug makers, biotech companies and biologics developers, to have validation documentation and implement controls such as audit trails and electronic signatures

White paper
31 January 2018

R&D-driven industries talk a lot about progressing towards the paperless laboratory. The ultimate aim is to capture and store all experimental, process, inventory and results data, from the earliest stages of discovery, through to manufacturing, QA/QC and even instrument management, in an electronic format

Webcast
04 September 2017

Join engineering virtual reality pioneers ESI | IC.IDO in this webcast as Eric Kam, Immersive Experience Product Marketing ESI, outlines the differences between 3D stereo CAD data viewing and immersive virtual prototyping.

White paper
03 August 2017

Data governance is an integral part of a regulated company’s quality system. Having a chromatography data system can simplify system administration and ensure regulatory compliance (including 21 CFR Part 11) and adherence to data integrity guidelines.

Pages

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Robert Roe looks at the changing ways that the HPC industry uses cloud computing technology

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Robert Roe reports on new technology and 30 years of the US supercomputing conference at SC18 in Dallas

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Sophia Ktori completes her two-part series on the use of artificial intelligence in healthcare research

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Robert Roe reports on developments in multiphysics simulation at the Global Altair Technology Conference

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Gemma Church reveals how simulation and modelling are aiding the design and development of a range of medical devices