Workshop Program and presentations

8:00 - 9:00 Registration
9:00 - 9:10 Opening remarks Dr. Ilya Kuselman
Chair of the Workshop International Advisory Committee, Israel
9:10 - 9:55 Plenary lecture:
The fitness for purpose of analytical methods: a laboratory method validation and related topics - abstract
Dr. Bertil Magnusson
SP Technical Research Institute of Sweden
9:55 -10:20 ISO/IEC 17025:2017 the New Upcoming Version - abstract
Mr. Ilan Landsman
Israel Laboratory Accreditation Authority (ISRAC)
10:20-10:45 Setting and Using Target Uncertainty in chemical measurement - abstract
Prof. Ricardo da Silva
Faculdade de Ciências da Universidade de Lisboa, Portugal
10:45-11:10 Evaluation of probabilities of false decisions at conformity assessment of test results - abstract
Dr. Francesca Pennecchi
Istituto Nazionale di Ricerca Metrologica (INRIM), Italy
11:10-11:25 Coffee break
11:25-11:50 Human error study as a part of method validation task - abstract
Dr. Ilya Kuselman
Independent Consultant on Metrology, Israel
11:50-12:15 Analytical test methods – to err is human. Practical application of risk management to analytical testing - abstract
Ms. Karen Ginsbury
PCI Pharmaceutical Consulting, Israel
12:15-12:50 Round-table discussion: Are there relationships between method validation, human errors and estimation of measurement uncertainty?

Presentation - A question on treatment of residual bias for measurement uncertainty (MU) evaluation
Dr. Ilya Kuselman

Presentation - Certified  Reference Materials  For Method Validation
Dr. Markus Obkircher
Moderator: Dr. Michela Sega
INRIM, Italy
12:50-13:30 Lunch
13:30-13:55 Validation of qualitative methods: Evaluation of repeatability and reproducibility - abstract
Prof. Emil Bashkansky
ORT Braude College, Israel
13:55-14:20 Handling different matrices in validation of analytical methods based on LC/MS - abstract
Dr. Anneli Kruve
University of Tartu, Estonia
14:20-14:45 Peak purity and spectral matching during validation of LC methods - abstract
Dr. Shula Levin
Waters (TC) Ltd., Israel
14:45-15:00 Coffee break
15:00-15:25 AQbD in practice: Risk assessment based on FMEA methodology is applied for complex sample preparations and chromatographic impurities separation - abstract
Presentation is not available
Dr. Bianca Avramovitch
Teva Pharmaceuticals Industries Ltd, Israel
15:25-15:50 Method validation, can the theory work in reality? Pharmaceutical industry experience - abstract
Dr. Orna Dreazen
Nextar Chempharma Solutions Ltd, Israel

Round-table discussion: How can validation be planned to provide a method user with maximum information?

Presentation - AOAC International - Guidelines for standard method performance requirements 2016
Dr. Ilya Kuselman

Presentation - Novel Services for Analytical Method Validation and Other Method Lifecycle Activities
Dr. Hellmuth Broda

Presentation - Challenges of validation of a GC method - matrix effect and deviation from linearity
Dr. Mikhail Zayats

Moderator: Dr. Raphy Bar
BR Consulting, Israel