1 – 2 February 2010 Paris, France
BIOMEDEVICE
Presentation on “Developing Effective Clinical Studies for Combination Products”
BIOMEDEVICE
Drug Device Combination Products
17-19 November 2009 in Prague, Czech Republic
Drug Device Combination Products
Presentation on “Drug/device borderline – latest developments”
Organised and led a workshop on “Post Market Surveillance for Drug-Device Combination Products”
Medtec Ireland
23 – 24 September 2009, Galway, Ireland
Medtec Ireland
Chairing the first day of the conference
Presentation on “Regulatory Framework for Combination Products in the EC “
Course on Regulation of Combination Products and Other Technologies in the EU
11 December 2008 at University of Cranfield, UK
Course on Regulation of Combination Products and Other Technologies in the EU
Lecture on “Issues and specifics in clinical development of combination products”
Drug Device Combination Products
27 – 29 October 2008, in Barcelona, Spain
Drug Device Combination Products
Organised and led a workshop on “Developing effective clinical studies for combination products”
Presentation on “Combination products: legal considerations in borderline determination and clinical implications” and “How have the revisions to the Medical Device Directive impacted on combination product approval?”
Event website
Drug Device Combination Products
4 – 5 December 2007 Brussels, Belgium
Drug Device Combination Products
Presentation on “Strategies for achieving the CE mark for combination products quickly and with minimal complexities”