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BSI Compliance Navigator: latest white paper- Ethical and trustworthy Artificial...

Jun 27th 2023
In 2021 the European Commission released the draft AI Act (AIA) (EC, Artificial Intelligence Act, 2021). Following the initial release, the AIA text has changed and developed as it has made ...
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Air Products is the only UK industrial gas supplier to offer liquid nitrogen com...

Feb 18th 2022
Air Products is proud to announce that it has been awarded Medical Device Regulation (MDR) EC Mark certificate for Medical Device liquid nitrogen for the UK.
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Chubb Life Science - Medical Device Regulation

May 28th 2021
On 26th May 2021, the new Medical Device Regulation (MDR) will be implemented in the European Economic Area as the legal basis for the manufacture of medical devices.
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Understanding Validation Training course launched by ITS

Feb 17th 2021
Are you trying to interpret and understand what validation means? If you read the regulatory requirements, either from the European, American, or other regulators, does it still leave you pu...
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Vaccine platform technologies to combat emerging infectious diseases

Apr 6th 2020
Encouraging progress is being made towards vaccine development against Covid-19. It is essential that we continue to incentivise and fund research into and development of these technologies.
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Precision medicine: ethics, regulation and patent law

Sep 2nd 2019
New genomic and proteomic analysis technologies allow for diagnosis and prognosis of patients with greater accuracy than ever before. However, this technology raises a number of ethical ques...
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Brexit Update

Aug 7th 2018
The UK Government is preparing for the UK’s exit from the European Union, and have published a number of documents to clarify our work to the Life Science sector.
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