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The top documents tagged [patient organisation]
Transparency: Should CF-care centers ”open their books” and publish treatment outcomes? PRO by Erik Wendel, Danish Cystic Fibrosis Association Hamburg
214 views
How to influence society? politicians partners in health policy (insurance companies) public opinion media industry & trade unions
213 views
Patient involvement in rare disease research
39 views
Emerging issues in Europe panel Dr Alastair Benbow VP and European Medical Director 6 June 2007, Brussels International Pharmaceutical Regulatory and Compliance
220 views
A testimony from young patients Timo Nerkko Finland Ceapir Budapest, October 25, 2010
218 views
Methodological Innovations in Qualitative Longitudinal Research Liam Berriman, Claude Jousselin, Ester McGeeney, Rachel Thomson, Susie Weller
221 views
Emerging issues in Europe panel Dr Alastair Benbow VP and European Medical Director
18 views
Transparency: Should CF-care centers ”open their books” and publish treatment outcomes? PRO
29 views
Methodological Innovations in Qualitative Longitudinal Research
36 views
Spectrum – Issue 42
233 views