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Please contact any of the experts here for more information about our capabilities and their expertise in the life sciences and healthcare sector in your jurisdiction.
Curated by our team of international life sciences experts, Synapse features the latest legal and regulatory developments you need to know about.
Latest insights
Life sciences & healthcare
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Orphan drug protection: clarification needed
25 October 2021
Briefing
Life sciences & healthcare
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UK medicines – Is the Northern Ireland Protocol now unsustainable?
14 October 2021
Quick read
Patents & innovation
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Taylor Wessing spearheads launch of new Trans-Pacific intellectual property guide
30 September 2021
by multiple authors
Patents & innovation
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The UK and the Trans-Pacific Partnership – Could patent conflicts ruin the deal?
Available in English and Japanese
31 August 2021
Briefing
Patents & innovation
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The EU torpedoes itself in cross-border patent disputes
6 May 2021
Briefing
Life sciences & healthcare
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Paul England and Simon Cohen launch new life sciences IP guide
23 March 2021
by Dr Paul England and Simon Cohen
Digital health
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mHealth apps – top tips for GDPR compliance
26 January 2021
Briefing
Life sciences & healthcare
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One Nucleus Genesis Digital 2020 – Key takeaways from our cell and gene therapy panel session
6 January 2021
Quick read
Life sciences & healthcare
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8+2+1 plus what? How UK data and market exclusivity rights will be affected from 1 January 2021
3 December 2020
Briefing
by Alison Dennis and Dr Paul England
Life sciences & healthcare
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Biologics and biosimilars litigation update
25 November 2020
Quick read
by Matthew Royle, Ph.D. and Dr. Nora E. Wessendorf, LL.M. (Washington)
Patents & innovation
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Why developments in global trade will highlight patent enforcement in the UK and Trans-Pacific countries
16 November 2020
Quick read
by multiple authors
Medical devices
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The medical device regulatory regime in Great Britain and Northern Ireland after 31 December 2020
3 November 2020
Tools and online services
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.
Please contact any of the experts here for more information about our capabilities and their expertise in the life sciences and healthcare sector in your jurisdiction.
