Following the UK’s exit from the European Union (EU), the government identified a unique opportunity to improve how medical devices and in vitro diagnostic medical devices (IVDs) are regulated in the United Kingdom.
Compliance Monitoring Process – from April this year the MHRA are piloting a different approach to the monitoring of companies that are referred to the MHRA’s IAG (Inspection Action Group) for failure to comply with the standards of Good Manufacturing Practice or Good Distribution Practice.
Prescribing and Dispensing – Rural GP practices can act as Dispensing Doctors which means they can perform both the Prescribing and Dispensing of medication if it would be difficult for their patients to access a local pharmacy.
UK licensed medicinal products and the challenges of exporting – Many clients contact us for information and help on expanding the scope of their WDA license to include the export UK licensed medicinal products without necessarily understanding the challenges of exporting UK licensed medicinal products.
