RP Refresher Training
The RP Refresher Training course is designed specifically for RPs and Deputy RPs as an annual refresher on the GDP guidelines plus additional areas applicable to RPs and their nominated deputies.
The MHRA’s Guide to Defective Medicinal Products – Part 2
In the world of pharmaceutical distribution, product recalls aren’t an occasional inconvenience—they’re an operational reality. And when they occur, the expectations on wholesale dealers are high. The MHRA’s guidance is clear: distributors sit at a pivotal junction in the recall process, and their preparedness can determine whether a quality issue stays contained or becomes a national problem.
The MHRA’s Guide to Defective Medicinal Products – Part 1: Overview
When quality issues arise in the lifecycle of a medicinal product, the consequences extend far beyond the pharmacy shelf. The MHRA’s latest 2026 guidance on defective medicinal products offers a comprehensive roadmap for managing these events with rigour, transparency, and patient safety at the centre.
Medical Devices: Conformity Assessment and the UKCA Mark
This article provides an overview of the recent MHRA update for UKCA conformity assessment for medical devices, with practical insights for regulatory, quality, and executive teams.
Are Audit clip boards and checklists obsolete?
Are your quality and audit team ready for the digital shift? Do they have the right mindset? The tools are there is it time to assess which ones are right for your organisation.
Major Changes to MHRA Medical Device Registration Fees
There is a hard stop to the change process, from 1st April the system will be operable, and the products registered at that point will decide the fees payable for 2026/27. So, there are a number of actions manufacturers and UKRPs will need to consider.