Articles

Results 1 to 5 of 15
Most popular |Most recent


Q&A: marketing authorisation for pharmaceuticals and medical devices in United Kingdom

United Kingdom - October 16 2020 This article answers some of the key legal and practical questions surrounding the grant of marketing authorisation for pharmaceuticals and medical devices in United Kingdom.

Ewan Townsend, Jackie Mulryne, Lincoln Tsang.

Q&A: the promotion and sale of pharmaceuticals and medical devices in United Kingdom

United Kingdom - October 16 2020 This Q&A covers the essential legal and practical considerations surrounding the promotion and sale of pharmaceuticals and medical devices in United Kingdom.

Ewan Townsend, Jackie Mulryne, Lincoln Tsang.

Q&A: pharma & medical device regulation in United Kingdom

United Kingdom - December 10 2019 A Q&A guide to pharma & medical device regulation in United Kingdom, covering the healthcare bodies and competent authorities, marketing authorisation, defective and unsafe products and much more.

Ewan Townsend, Jackie Mulryne, Lincoln Tsang.

Q&A: marketing authorisation for pharmaceuticals and medical devices in United Kingdom

United Kingdom - December 10 2019 This article answers some of the key legal and practical questions surrounding the grant of marketing authorisation for pharmaceuticals and medical devices in United Kingdom.

Ewan Townsend, Jackie Mulryne, Lincoln Tsang.

Clinical trial consents under the EU GDPR: where do we stand?

European Union, United Kingdom - June 28 2018 The General Data Protection Regulation (GDPR) entered into force on 25 May 2018 and, in the absence of any transition period, companies are now…

Ewan Townsend, Jackie Mulryne, Kathy Harford, Richard Dickinson.