||

September 2009 Presentations

September 2009 Presentations

 

Speaker

Title of Talk

Presentation

Introduction
Philip Minor Welcome address  
Clare Morris Overview of SoGAT BV XXI
Session 1: Higher order standards for clinical virology
Clare Morris Development of an HIV-2 RNA International Standard
Jacqueline Fryer An update on the development of the proposed 1st WHO International Standards for HCMV and EBV for NAT-based assays
Marcia Holden   Development of a NIST Standard Reference Material for Cytomegalovirus
Michael Chudy Proposal for the development of an international reference preparation for hepatitis D virus RNA
Session 2: JC and BK virus standardisation
Paola Cinque Measurement of JCV DNA in CSF for diagnosis and monitoring of PML
Hans Hirsch Polyomavirus Diagnostics: In Need of International Quantitation Standards
 
Anton van Loon The QCMD external quality assessment programme for molecular detection and quantification of BK virus and JC virus
Eugene Major Assays for the detection of human polyomavirus DNA in blood, CSF, and brain tissue, at the National Institutes of Health
 
Session 3: Working reagents and reference panels for clinical virology
Heather Carré Ensuring quality of NAT based assays in routine clinical virology
Renée Howell Standardization of Human Papilloma Virus (HPV) DNA testing
Saeko Mizusawa Preparation of Reference Panels for in vitro Diagnostic Tests in Japan
Session 4: Reference materials for bacteria and other pathogens
Kate Templeton Challenges in quality control in molecular diagnosis of bacterial targets
Anna Gottlieb Working reagents for bacteriology NATs – first steps
Session 5: EQAS / Proficiency testing / Data reporting
Christine Ginocchio Results of the College of American Pathologists (CAP) Proficiency Program for CMV, EBV, and BKV Viral Load Testing
Heinz Zeichhardt The benefit of INSTAND EQAS for improvement and standardization of CMV and EBV genome detection assays - EQAS for new influenza A(H1N1)
 
Isabella Abbate Italian multicenter comparative study of EBV quantification using Real-time PCR
Fausto Baldanti “QCMD 2007 Human CMV DNA EQA Programme”: Results from a multicenter Italian working group
Joy Kean A Performance Assessment of 12 UK-Wide Laboratories In-House Real Time PCR Methods for 8 Viral Targets
Vivienne James UK NEQAS for Microbiology Quality Assessment Programmes for HPV and MRSA. Effect of change to assessment categories for HBV DNA  View Presentation
Francesca Luciani Quantification of HCV RNA in a Multicenter Study: Implications for the management of HCV Genotype1-infected patients        
Joe Vincini HPA QC ‘Result Reporting System’ Software Development View Presentation
Session 6: Technical aspects / assay validation / regulation
Angela Caliendo CMV Commutability Studies: All Calibrators are not Born Equal  
Alexis Dumoulin Adaptation of a real-time PCR assay for the detection of the polyomavirus BK to newly available sequences  
Francisco Martínez Murillo Regulating IVDs without International Standards  
Simon Carne Solutions for the provision of difficult to source control materials for In-House real-time assays  
Session 7: Prioritising the development of future standards
Jacqueline Fryer Prioritising the development of future standards (followed by general discussion)  
View Presentation