HPRA Update for Medical Devices
HPRA have today (23rd March 2026) released their latest update and the Mandatory Use of EUDAMED modules for medical devices
Cogent Accredited MHRA Gold Standard Training for Responsible Persons
In pharmaceutical distribution, excellence isn’t accidental – it’s engineered through knowledge, responsibility, and a commitment to doing things the right way. For Responsible Persons (RPs) and those aspiring to the role, that commitment begins with training that is not only comprehensive, but recognised, trusted, and built to last.
RP Refresher Training
In the world of pharmaceutical distribution, standing still is not an option. Regulations evolve, expectations sharpen, and the responsibility carried by Responsible Persons (RPs) continues to grow. Maintaining clarity, confidence, and compliance requires more than experience alone – it requires regular refinement.
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.