Notification Fees for Great Britain and Northern Ireland
The fees for submitting a notification are a set out in The Electronic Cigarettes etc. (Fees) Regulations 2016. The MHRA consulted on the level of these fees in January 2016.…
Reporting adverse incidents: intraocular lenses
Guidance on how to report adverse incidents with intraocular lenses. To be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1.
UK-Canada Trade Continuity Agreement (TCA)
As CETA ceased to apply to the United Kingdom from 1 January 2021, Canada and the UK agreed on an interim agreement until a comprehensive free trade agreement was in…
Adverse incidents: in vitro diagnostic (IVD) blood glucose meters
IVD blood glucose meters – POCT or home useTo be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1 which sets out the general adverse…
Good laboratory practice (GLP) facilities: risk-based quality assurance
This guidance covers:risk-based GLP quality assurance programmesthe risk assessment life cycledifferent types of inspectionsSee the detailed guide on good laboratory practice (GLP) for safety tests on chemicals for more information.We…
