Describe what type of information materials should be provided (writing and/or translation, other adaptation) and if the informed consent for participating is required?
Manufacturer data, effectiveness studies, observational studies, applicability studies, clinical experts, user information, patient organisations, HTA-reports, discussion forums in web, as well as grey literature, hand-searches and conference proceedings,
National or local judgement
Liberati A. et al. 1997; Busse R. et al. 2002; Kristensen FB et al. 2001; Draborg E et al. 2005