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Standardisation of Genome Amplification Techniques
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September 2009 Presentations
September 2009 Presentations
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September 2009 Presentations
Speaker
Title of Talk
Presentation
Introduction
Philip Minor
Welcome address
Clare Morris
Overview of SoGAT BV XXI
View Presentation
Session 1: Higher order standards for clinical virology
Clare Morris
Development of an HIV-2 RNA International Standard
View Presentation
Jacqueline Fryer
An update on the development of the proposed 1st WHO International Standards for HCMV and EBV for NAT-based assays
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Marcia Holden
Development of a NIST Standard Reference Material for Cytomegalovirus
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Michael Chudy
Proposal for the development of an international reference preparation for hepatitis D virus RNA
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Session 2: JC and BK virus standardisation
Paola Cinque
Measurement of JCV DNA in CSF for diagnosis and monitoring of PML
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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
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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
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Renée Howell
Standardization of Human Papilloma Virus (HPV) DNA testing
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Saeko Mizusawa
Preparation of Reference Panels for
in vitro
Diagnostic Tests in Japan
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Session 4: Reference materials for bacteria and other pathogens
Kate Templeton
Challenges in quality control in molecular diagnosis of bacterial targets
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Anna Gottlieb
Working reagents for bacteriology NATs – first steps
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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
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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
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Fausto Baldanti
“QCMD 2007 Human CMV DNA EQA Programme”: Results from a multicenter Italian working group
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Joy Kean
A Performance Assessment of 12 UK-Wide Laboratories In-House Real Time PCR Methods for 8 Viral Targets
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Vivienne James
UK NEQAS for Microbiology Quality Assessment Programmes for HPV and MRSA. Effect of change to assessment categories for HBV DNA
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Francesca Luciani
Quantification of HCV RNA in a Multicenter Study: Implications for the management of HCV Genotype1-infected patients
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Joe Vincini
HPA QC ‘Result Reporting System’ Software Development
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Session 6: Technical aspects / assay validation / regulation
Angela Caliendo
CMV Commutability Studies: All Calibrators are not Born Equal
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Alexis Dumoulin
Adaptation of a real-time PCR assay for the detection of the polyomavirus BK to newly available sequences
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Francisco Martínez Murillo
Regulating IVDs without International Standards
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Simon Carne
Solutions for the provision of difficult to source control materials for In-House real-time assays
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Session 7: Prioritising the development of future standards
Jacqueline Fryer
Prioritising the development of future standards (followed by general discussion)
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View Presentation
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