Category: Medical Device Regulations

This is the fifth of our posts looking at the main points of contention so far at Committee Stage in the House of Lords for the Medicines and Medical Devices Bill 2019-20. [Part I available here, Part II available here, Part III available here, Part IV available here]   The ever present issue of balancing … Continue reading “Lords Discuss Prescribing Rights and Medical Device Innovation in Fifth Committee Session on the Medicines and Medical Devices Bill”

This is the fourth post looking at the main points of contention so far at Committee Stage in the House of Lords for the Medicines and Medical Devices Bill 2019-20. [Part I available here, Part II available here, Part III available here] Another week, another Committee session in the House of Lords on the Medicines … Continue reading “Lords Challenge Data Sharing and Emergency Powers in Short 4th Session of Medicines and Medical Devices Bill Committee”

This is the third post looking at the main points of contention so far at Committee Stage in the House of Lords for the Medicines and Medical Devices Bill 2019-20. [Part I available here, Part II available here] In another busy week of Brexit-related Parliamentary business, two further Committee sessions took place in the House … Continue reading “Lords keep up pressure on Government over Medicines and Medical Devices Bill in 2nd & 3rd Committee Stage Sessions”

This is the second of our posts looking at the main points of contention so far at Committee Stage in the House of Lords for the Medicines and Medical Devices Bill 2019-20. [Part 1 available here] In this post, which reports on the first session of the Lords Committee Stage for the Medicines and Medical … Continue reading “Lords take Government to task over future of medicines and medical devices regulation: Part 2”

This is the first of a series of posts looking at the main points of contention so far at Committee Stage in the House of Lords for the Medicines and Medical Devices Bill 2019-20. [Part 2 available here] The second session of the Lords Committee Stage on the Medicines and Medical Devices Bill starts today … Continue reading “Lords take Government to task over future of medicines and medical devices regulation: Part I”

The shape of the post-Brexit regulatory landscape has been the subject of much discussion in recent months. With the end of the transition period looming and the Government remaining scant on details, many academics and stakeholders have been exploring the possibilities. Reform, a Westminster think tank for public service reform, invited Dr Laura Downey, Dr … Continue reading “Beyond Brexit: Smart Regulation for Investment and Patient Safety”

Originally posted here. Executive summary Patient and user safety with regards to medical devices is paramount. This should be prioritised in situations where there are competing considerations such as “attractiveness of the UK” as to the conduct of clinical trials and supply of medicines and medical devices. The existing regulatory framework for medicines and medical … Continue reading “Briefing note: Medicines and Medical Devices Bill (July update)”

Although the Medicines and Medical Devices Bill received its first reading in the House of Commons on the 13th of February, progress on the Bill was interrupted by the Covid-19 crisis in March 2020. The Bill has since been re-introduced, passing quickly through the House of Commons. Professor Muireann Quigley, Professor Jean McHale, Dr Rachael … Continue reading “Written evidence: We shouldn’t rush the Medicines and Medical Devices Bill”

This piece was originally posted on the Birmingham Law School news page. The committee stage of the Medicines and Medical Devices Bill 2019-20 resumed this week. The government has brought forward this new legislation to regulate medicines and medical devices following Brexit. Progress on the Bill paused in March 2020 due to the Covid-19 crisis, … Continue reading “Medicines and Medical Devices Bill 2019-20: Patient safety must be the priority”

Currently, a large part of the UK’s regulatory regime governing medicines and medical devices is derived from EU law. The Medicines and Medical Devices Bill (MMDB) 2019-20 sets out a suite of provisions for the regulation of medicines and medical devices in the UK at the end of the EU exit transition period, currently 31 … Continue reading “Briefing note: How we can improve the Medicines and Medical Devices Bill?”