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Results:1-10 of 46

New MHRA guidance on Brexit implementation period and the lifesciences sector
  • CMS
  • United Kingdom
  • August 15 2018

On 6 August 2018, the MHRA released new guidance on what the Brexit implementation period means for the lifesciences sector, as well as an update on


EU institutions agree text of new Medical Devices legislation
  • CMS
  • European Union
  • May 27 2016

On Wednesday 25 May the EU institutions reached agreement on the draft texts for the revised Medical Devices Regulation and In Vitro Diagnostics


Clearcast not subject to Judicial Review
  • CMS
  • United Kingdom
  • May 19 2016

In an important decision for all UK advertisers, but especially those advertising medical devices, the High Court has found that Clearcast is not


The Antidote - Winter 2015
  • CMS
  • OECD, European Union
  • December 4 2015

The intended two new EU Regulations, one for devices and one for diagnostics, will replace the current three Directives. A series of fi ve blocks of


Revision of the EU medical device legislation enters trilogue negotiations
  • CMS
  • European Union
  • October 19 2015

Negotiations between the European Parliament, European Council and European Commission to agree on the proposed revision of the EU medical devices


UK proposes a "Sunshine Rule" for 2016 to improve transparency between NHS healthcare professionals and industry
  • CMS
  • United Kingdom
  • August 27 2015

The Secretary of State for Health has proposed implementing a rule requiring NHS healthcare organisations to keep registers of any gifts that their


ASA adjudications snapshot April 2015
  • CMS
  • United Kingdom
  • May 29 2015

A TV ad promoted a topically applied gel used to relieve joint pain, stating it was “Drug Free” and “doesn’t contain any drugs”. The complainant, a GP


Ukraine cancelled VAT and additional import duty on certain medicines
  • CMS
  • Ukraine
  • May 21 2015

In March 2015 Ukraine began allowing state procurement of certain medicines and medical devices to be conducted via international organizations such


Proposed changes to the Eucomed Code
  • CMS
  • European Union
  • February 20 2015

Medical device and IVD companies subscribing to the Eucomed or counterpart national business ethics Codes will have to start preparations to cease


Revision of the Swiss Therapeutic Products Act
  • CMS
  • Switzerland
  • February 20 2015

As at the start of 2015, three different versions exist of the revised Swiss Therapeutic Products Act, which will change the law on discounts and