A selection of presentations made by the EDMA Secretariat and the members at various conferences and events.

Diabetes Case Study on EU Advocacy
by Dagmar Kownatka, Chair EDMA Diabetes Task Force, Roche
3 December 2008, Athens, Greece
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Clinical and Economic IVD Benefits
by Gloria Galán, EDMA Communications &  PA Manager
2as JIQLAC
9 November 2007,Lisbon, Portugal
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Instructions for Use (IFU) - How to provide them to the Users?
by Benny Ons, Chairman EDMA Regulatory Affairs Committee, pharma.be Diagnostics - BD
Informa labelling and Packaging Compliance for medical devices and IVDs
25 September 2007,Brussels, Belgium
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Specific labelling requirements under the In Vitro diagnostic medical devices Directive
by Karen Howes, EDMA Director Regulatory Affairs
Informa labelling and Packaging Compliance for medical devices and IVDs
25 September 2007,Brussels, Belgium
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Working with Policy Makers: EDMA advocacy experience with EU institutions
by Gloria Galán, EDMA Communications & PA Manager
8th Czech National Congress of Clinical Biochemistry
24 September 2007,ČeskéBudějovice, Czech Republic
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EQA Contribution and Industry Expectations
by Dr. Claude Giroud, Chairman EDMA Standardisation, Quality & Risk Management Task Force
8th Czech National Congress of Clinical Biochemistry
24 September 2007,ČeskéBudějovice, Czech Republic
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The EDMA Code of Ethics
by Gloria Galán, EDMA Communications &  PA Manager
Roche Diagnostics EMEA, Compliance Network Meeting
20 September 2007,Mannheim, Germany
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Esperienza europea sui dispositivi medico-diagnostici in vitro
by Christine Tarrajat, EDMA Director Genera 
Conferenza nazionale sui dispositivi medici
8 June 2007,Rome, Italy
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Emerging Technical Developments in IVDs
by Christine Tarrajat, EDMA Director General
Hellasmes Workshop
11 May 2007,Athens, Greece
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In Vitro Diagnostic a Keystone in Healthcare
by Jean-François de Lavison, EDMA President, Christine Tarrajat, EDMA Director General, and Gloria Galán, EDMA Communications and Public Affairs Manager
EDMA Meets Health Commissioner Kyprianou
2 May 2007
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Industry Perspective
by Karen Howes, EDMA Regulatory Affairs Director
EUROGENTEST Workshop on Genetic Testing and the IVMDD
24 April 2007
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The Central role of the Medical Laboratory
by Christine Tarrajat, EDMA Director General
5th National Congress on Laboratory Medicine
2-5 November 2006,Brasov, Romania
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Characterisation of the IVD Market and Industry
by Jean-François de Lavison, EDMA President
II Apifarma Forum
24 October 2006,Porto, Portugal
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IVD: Expenditure or Investment in Health
by Christine Tarrajat, EDMA DIrector General
II Apifarma Forum
24 October 2006,Porto, Portugal
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Manufacturers Perspective
by Alisha McReynolds
Prion 2006
5 October 2006,Turin, Italy
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In vitro diagnostic Medical Devices - New Developments and Future Prospects
by Karen Howes, EDMA Director Regulatory Affairs
Topra Symposium
3 October 2006,Amsterdam, The Netherlands
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EQA Contribution and Industry Expectations on Quality Assurance and Control in Medical Analysis
by Claude Giroud, Chairman EDMA Standardization, Quality and Risk Management Task Force, Bio-Rad
EQALM Symposium,
12 September 2006,Geneva, Switzerland
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