Bergen, Norway, 8-9 October, 2015
The presentations in this page have been archived and are no longer available.
| Topic | Speaker |
|---|---|
| Session 1: Analytical quality specifications | |
| The Milan 2014 consensus document | Sverre Sandberg |
| Biological variation database, time for an update? | Bill Bartlett |
| Common performance goals in EQA, is it possible? | Graham Jones |
| Session 2: Point-of-care testing | |
| Benefits and disadvantages of POCT | Gunnar Nordin |
| The challenges of quality assessment for POCT | Anne Stavelin |
| How to evaluate the performance of POC instruments? | Grete Monsen |
| EQA provider experience with POCT | Pierre-Alain Morandi |
| Session 3: Adam Uldall Lecture | |
| Performance criteria of point-of-care testing in modern medicine | Sverre Sandberg |
| Session 4: Harmonisation | |
| European harmonization initiatives | Ferruccio Ceriotti |
| 40 years EQA experience – on the road to harmonisation? | Michael Spannagl |
| Update on UK Pathology Catalogue project | Finlay Mackenzie |
| Session 5: The members' session: Abstracts | |
| Acceptance sampling theory applied to EQA sample homogeneity testing | Wim Coucke |
| ProMeQualLab - Project of Laboratory Quality Improvement for Portuguese Speaking Countries | Ana Faria |
| Variables in the design of bone marrow morphology proficiency testing program: A ten year review of results from the Institute for Quality Management in Healthcare (IQMH), Canada | Ruth Padmore |
| How to determine acceptability limits based on biological variation in External Quality Assessment Schemes (EQAS): lymphocyte subsets as a case study | Mohamed Rida Soumali |
| External quality assessment programs in mycology - development of a scheme for galactomannan antigen detection | Christine Walton |