The Medicines and Healthcare Products Regulatory Agency (MHRA) has produced a series of free e-learning modules for healthcare professionals.For medical devices, e-learning programmes are available from Health Education England.
Supply of authorised medicines to Northern IrelandMedicines for the Northern Ireland market must follow the EU acquis in accordance with Annex 2 of the Northern Ireland Protocol with a pragmatic…
OverviewIn order to sell medicines in the EU, EU-based online sellers must register, comply with relevant requirements and display an EU common logo linked to the competent authority of the…
Guidance on how to report adverse incidents with biological/mechanical surgical heart valves. To be read in conjunction with the guidelines on a medical devices vigilance system MEDDEV 2.12/1.
We have previously published specific software guidance on medical device stand-alone software including apps.Types of software likely to be a medical device‘Software’ is defined as a set of instructions that…
