We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Principle One has been with ACE since our earliest days. We speak to CEO Maggie Scott about how this has helped the company develop and grow.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
Bristol-Myers Squibb Pharmaceuticals Limited has informed the MHRA that a potential product quality issue has been detected, relating to incomplete crimping of the metal crimp cap of OPDIVO 10mg/mL concentrate for solution for infusion (nivolumab) (1VLX10ML).
The Accelerated Capability Environment is a unit within the Homeland Security Group tackling public safety and security challenges arising from evolving digital and data technology. ACE is part of the Home Office .
Volume 52 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 10 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 13 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 32 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 23 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Volume 33 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
Healthcare professionals should complete this form for children who are carriers of the cystic fibrosis (CF) gene within 24 hours of giving results.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Volume 35 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 22 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.