Validation Guidance for Medical Laboratories IBMS LabMed MHRA UKAS
Validation Guidance for Medical Laboratories provides practical guidance for validating and verifying in vitro diagnostic devices in line with ISO 15189 requirements. It covers manufacturer claim verification, off-label use, laboratory-developed tests, RUO reagents and emerging technologies, with a risk-based framework, practical workflow and real-world case studies to support safe, reliable and fit-for-purpose testing
An IBMS Quality SAP Webinar. Updates to the Royal College of Pathologists (RCPath) Retention and Storage of Pathological records and specimens guideline – version 6 issued October 2025
A presentation will be led by IBMS Vice President Debra Padgett, Clinical Pathology Lead and Lead Healthcare Scientist, Northumbria Healthcare NHS Foundation Trust.
