BACKGROUND

Aiming at connecting excellence in clinical research on a global horizon, ICN strives to harmonize the standards for facilitating collaboration among members, in particular in multinational, multicentre clinical studies.

This workgroup targets to work out the objectives and scope of harmonization, and to formulate a realistic implementation plan with solid deliverables. Possible dimensions may include quality standard and quality control, data and IPR ownership, and general contract terms.

MEMBERS
Convener:

Dr Britta Lang Clinical Trials Unit Freiburg, Albert-Ludwigs-University of Freiburg, University Hospital Freiburg, Freiburg

Contributors:

Academic Clinical Research Office, Khon Kaen
Baim Institute for Clinical Research, Boston
Cambridge Clinical Trials Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge
University of Istanbul Center of Excellence for Clinical Research, Istanbul
Centre for Clinical Trials Essen, Essen
Clinical Trial Center, China Medical University Hospital, Taichung
Clinical Trial Center, Department of Research, Hualien Tzu Chi General Hospital, Hualien
Clinical Trials Center, University of Zurich and University Hospital Zurich, Zurich
Clinical Trials Centre, The University of Hong Kong, Hong Kong
Infectious Diseases Institute, Kampala
Institute for Advancement of Clinical and Translational Science, Kyoto University and Kyoto University Hospital, Kyoto
Medical University of Graz, Graz
Muenchner Studienzentrum, Technical University Munich, School of Medicine, Munich
Oncology Clinical Trials Unit, College of Medicine, University of Ibadan/University College Hospital Ibadan, Ibadan
Research Institute for Healthcare and Medical Management of Moscow Healthcare Department, Moscow
Shanghai Clinical Research Center, Shanghai
University of South Australia, Adelaide