Life Sciences By Alison McAdams We have defended the majority of significant pharmaceutical/medical product liability cases in the UK over the last four decades, including Opren, Whooping Cough Vaccine, Benzodiazepines, HIV Haemophilia, Oral Contraceptives, MMR and the Hepatitis C…
Medical Device Reform – creating a landscape for the future By Alison McAdams Following its public consultation on the future regulation of medical devices, the Medicines and Healthcare products Regulatory Agency (MHRA), the UK’s regulator, has announced its plans to improve patient safety and encourage innovation.
New template clinical research agreements published by the Health Research Authority By Andrew Johnston The Health Research Authority (“HRA ” ) has published its eagerly awaited template agreements for commercial non-interventional research being carried out at NHS sites. These are the first UK templates designed for this purpose. The HRA has also…
“Better regulation…for better clinical trials…for better health” – MHRA consultation on the future of UK clinical trials By Alison McAdams Clinical trials are a critical element of medical research. They are key for achieving advances in treatment by demonstrating if medicines are safe and effective as has been seen with the successful introduction of new vaccines and therapeutics…
Product Liability Decision Finds for Pinnacle Metal on Metal Hip Manufacturer By Alison McAdams In the much-anticipated Depuy Pinnacle Metal on Metal (MoM) Hip Litigation decision, Mrs Justice Andrews has found that the defendant manufacturer was not liable to the claimants. In Gee and others v Depuy International Limited [2018] EWHC 1208…
Clouded judgment: when is software regulated as a medical device? By Alison McAdams Technology is revolutionising medicine and software is increasingly used in healthcare to help both patients and clinicians in their decisions. But software, in all its forms and applications, presents significant challenges both to designers and…
Anti-corruption lessons for MedTech companies following first conviction for failing to prevent bribery By Alison McAdams Life science and MedTech companies of all sizes should review their anti-corruption procedures following the outcome of the first contested case under section 7 of the Bribery Act 2010 (the "Act"). After a two-day trial at Southwark Crown Court,…
Medical device business practice changes: are you ready? By Alison McAdams Manufacturers of medical devices should note the changes being phased in by the Association of British Healthcare Industries ("ABHI") this year, which will align the UK approach with that of MedTech Europe by January 2019, and they should ensure…