Events during September 2023

What’s in the new precompatibility guidelines?

Highlights from the 2022 Annual SHOT Report: lessons learnt and learning from excellence

Reporting haemovigilance incidents is vital to the ongoing learning from errors and improvements of quality management systems in transfusion. It is a statutory reguirement of the Blood Safety and Quality Regulations (2005) (as amended) and the data collected is used by both MHRA and SHOT to analyse and demonstrate key learning opportunities.

This presentation will give an overview of the legal requirements of the BSQR and the Good Practice Guide. Common isnspection findings will be presented and practical learning from SABRE reports will be shown. Common issues associated from reports received will be discussed and tips given as to how to improve the reporting of haemovigilance data.

An overview of the UKTLC collaborators and history of the UKTLC. An introduction to the new standards and the evidence supporting these and the findings of the 2022 UKTLC survey.

This session provides an overview of the key changes to the ISO 15189 standard and explains the UKAS transition process including deadlines and actions to be taken by accredited organisations.

The same session is being run on Monday, Tuesday and Thursday to ensure as many delegates as possible are able to attend.

Using accreditation to support the validity of test results: pre-examination requirements of ISO 15189:2022

The principles of validation and verification have long been established and laboratories are generally familiar with these although there remain some issues which are commonly seen within verification reports during assessments. Some of these require some further attention and discussion, including consideration of sample type, verification across multiple sites and approaches used when upgrading analysers. Alongside these common issues, ISO 15189:2022 has now been issued with assessments to become mandatory to the new standard from January 2024 and whilst the principles of validation and verification are generally unchanged, there are some differences which will require review of internal procedures and approaches to verification. Awareness of these changes will form a part of the presentation, along with issues commonly seen, being hoped these will promote some thought as to how laboratories can consider the local approaches used.

Pathology services across the UK are increasingly working together as formal or informal networks, to support improved patient care.

This session provides an overview of accreditation options and considerations for pathology networks.

ISO15189:2012 had reached its periodic review date and there was international consensus that it needed revision. The new version was published on 6th December 2022 and there are some key changes which include an emphasis on a patient-focused approach and to promote the welfare of patients - i.e. putting the patient at the heart of the service. There is also more emphasis on a risk-based approach to the Quality Management system. In addition, ISO 22870 (POCT) has been incorporated into ISO 15189:2022.

This presentation will review POCT definitions, highlight key considerations for currently accredited POCT services and also for organisations considering applying for accreditation to include (or extend) POCT in their scope.

POCT is referenced implicitly throughout ISO 15189:2022 and with additional distinct requirements as an Annex A.

The presentation will discuss generic POCT services, and highlight considerations on both current POCT services and also emphasise considerations for planning new POCT services, and that overall, when compared with ISO 22870:2016, things have not changed as much as one would think. Principles are similar, and POCT could even be considered as another specialty within pathology, regardless of where it is or managed from.

Post-pandemic respiratory viral infections in hospitals