This is an official blog of the Medicines and Healthcare products Regulatory Agency (MHRA).
We regulate medicines, medical devices and blood components for transfusion in the UK.
Recognised globally as an authority in our field, MHRA plays a leading role in protecting and improving public health and supports innovation through scientific research and development.
If you’re working to develop and submit applications to MHRA for marketing authorisations and clinical trial authorisations, you need to keep up to date with the latest regulatory thinking and be able to easily find tips and tricks to avoid common pitfalls.
We'll give you regular updates from our experts who work right across the regulatory process. They’ll share their top tips, insights and experience on a range of topics to help you stay informed. We'll also be inviting you to discuss your views on our work and how we can develop this into a useful and informative blog.
See our comments and moderation policy.