WP 1: Activities
1.1  Meeting reports of Industry Advisory Committee
1.2  Meeting reports of Priority Review Committee
1.3  Standard Operating Procedures
1.4  Study protocols and annual study accrual figures
1.5  Analysis of the conduct of clinical studies

WP 2: Activities
2.1 Comparison of current core data sets
2.2 Decision regarding final desired data sets
2.3 New data collection forms
2.4 Clinical trials database
2.5 First clinical trial to be implemented in CT database

WP 3: Activities
3.1  Report on national legislation of EU Directive
3.2  Report on Informed Consent and Data Protection in the context of transnational SCT research

WP 4: Activities
4.1 Portal structure and contents consensus
4.2 Portal basic layout and structure creation
4.3 Testing of Portal
4.4 Implementation of portal guidelines & contents;  Inventory of all data bases that need to be linked
4.5 Use of portal by research infrastructures and partners
4.6 Link with AGNIS project

WP 5: Activities
5.1 Inventory of existing bio-statistical literature
5.2 Establish consensus on exchange of methods and data
5.3 Create infrastructure on the portal for exchange of  data
5.4 Incorporate interactive visualization of statistical analyses

WP 6: Activities
6.1 Project Presentation
6.2 Launch of website
6.3 Establish a communications platform for sourcing information on project activities for the website 
6.4 Key donor/patient websites linked to the CLINT  website
6.5 Project information bulletins

WP 7: Activities
7.1 Initial plan for using and disseminating knowledge
7.2 Meetings of CLINT Steering Committee and ongoing internal assessment and review
7.3 Periodic reporting to Commission
7.4 Final plan for using and disseminating knowledge
7.5 Report on raising public participation and awareness