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Curated by our team of international life sciences experts, Synapse features the latest legal and regulatory developments you need to know about.
UK medicines – Is the Northern Ireland Protocol now unsustainable?
Taylor Wessing spearheads launch of new Trans-Pacific intellectual property guide
作者
The UK and the Trans-Pacific Partnership – Could patent conflicts ruin the deal?
Available in English and Japanese
Paul England and Simon Cohen launch new life sciences IP guide
作者 Dr Paul England 以及 Simon Cohen
One Nucleus Genesis Digital 2020 – Key takeaways from our cell and gene therapy panel session
8+2+1 plus what? How UK data and market exclusivity rights will be affected from 1 January 2021
作者 Alison Dennis 以及 Dr Paul England
Biologics and biosimilars litigation update
作者 Matthew Royle, Ph.D. 以及 Dr. Nora E. Wessendorf, LL.M. (Washington)
Why developments in global trade will highlight patent enforcement in the UK and Trans-Pacific countries
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The medical device regulatory regime in Great Britain and Northern Ireland after 31 December 2020
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EU Medical Device Regulation guides
The implementation of the EU Medical Device Regulation (MDR) and the EU In-Vitro Diagnostic Regulation (IVDR) is fast approaching, arriving in May 2021 and May 2022 respectively.
Our two comprehensive guides provide clarity for medical device and IVD companies who may find the sheer size and complexity of the regulations a substantial hurdle to their international expansion plans.
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