Thirty-eight million people contact a medical device every day in the UK. The UK has over 3000 companies employing 76 000 people in medical technology. Currently valued at £17 billion and growing at rates exceeding 6%, the UK has remained a leader in medical device innovation. Governed under the European Union (EU) Medical Device legislations, it is demonstrated that this model, and the UK's continued membership accounts to an optimal balance between safety and risk with early access to new innovation. Leaving the EU would have a detrimental effect on UK businesses where EU legislation is used for market access. With the cost of regulation increasing, and the cost of products being forced to decrease, many UK businesses will no longer find ...
Background: On 31 January 2020, the United Kingdom (UK) formally left the European Union (EU). Only ...
INTRODUCTION: The UK Pharmaceutical Industry is arguably one of the most important industries to con...
It has been suggested that we are entering a new era in medical device regulation in Europe. This pa...
Thirty-eight million people contact a medical device every day in the UK. The UK has over 3000 compa...
ObjectivesTo identify the potential opportunities and risks around future UK regulatory reform of me...
OBJECTIVES To identify the potential opportunities and risks around future UK regulatory reform o...
Following a series of major scandals over the past two decades, the medical device industry is now u...
With the exit of the UK from the European Union and the European Union Regulation 201/745 coming int...
At the time of writing the UK is faced with two of the largest challenges to its international statu...
ABSTRACT Introduction: Favoring innovation by making timely medical technology available to people ...
While policy attention is understandably diverted to COVID-19, the end of the UK's post-Brexit ‘tran...
The United Kingdom’s Medicines and Medical Devices Act (MMD Act) 2021 received royal assent on 11 Fe...
The symposium in this issue of Law, Technology and Humans brings together a range of scholars lookin...
The recent COVID-19 crisis, as well as the resulting international response, have demonstrated the i...
The process of leaving the European Union (EU) will have profound consequences for health and the Na...
Background: On 31 January 2020, the United Kingdom (UK) formally left the European Union (EU). Only ...
INTRODUCTION: The UK Pharmaceutical Industry is arguably one of the most important industries to con...
It has been suggested that we are entering a new era in medical device regulation in Europe. This pa...
Thirty-eight million people contact a medical device every day in the UK. The UK has over 3000 compa...
ObjectivesTo identify the potential opportunities and risks around future UK regulatory reform of me...
OBJECTIVES To identify the potential opportunities and risks around future UK regulatory reform o...
Following a series of major scandals over the past two decades, the medical device industry is now u...
With the exit of the UK from the European Union and the European Union Regulation 201/745 coming int...
At the time of writing the UK is faced with two of the largest challenges to its international statu...
ABSTRACT Introduction: Favoring innovation by making timely medical technology available to people ...
While policy attention is understandably diverted to COVID-19, the end of the UK's post-Brexit ‘tran...
The United Kingdom’s Medicines and Medical Devices Act (MMD Act) 2021 received royal assent on 11 Fe...
The symposium in this issue of Law, Technology and Humans brings together a range of scholars lookin...
The recent COVID-19 crisis, as well as the resulting international response, have demonstrated the i...
The process of leaving the European Union (EU) will have profound consequences for health and the Na...
Background: On 31 January 2020, the United Kingdom (UK) formally left the European Union (EU). Only ...
INTRODUCTION: The UK Pharmaceutical Industry is arguably one of the most important industries to con...
It has been suggested that we are entering a new era in medical device regulation in Europe. This pa...