“…Other types of data analysed (14% (n = 27) of the studies) included project plans, operational guidelines and data, e.g. a framework for health needs assessment (n = 7) [74][75][76][77][78][79][80], press releases and news stories (n = 5) [81][82][83][84][85], definitions produced by NGOs (used as operational constructs in the studies) (n = 4) [86][87][88][89][90], clinical guidelines and guidance on clinical guideline development (n = 4) [74,80,91,92], educational resources and information for clinicians (n = 3) [93][94][95], unspecified contributions of background information by NGO members (n = 3) [96][97][98], contracts (n = 3) [76,77,99], an interview transcript (n = 1) [82], and workshop proceedings (n = 1) [100]. The clinical data analysed in 5% of the studies were collected by NGOs via drug distribution and treatment monitoring systems and health monitoring information systems (patient records).…”