Beyond the FDA PRO guidance: steps toward integrating meaningful patient-reported outcomes into regulatory trials and US drug labels
- PMID: 22583448
- DOI: 10.1016/j.jval.2012.03.1385
Beyond the FDA PRO guidance: steps toward integrating meaningful patient-reported outcomes into regulatory trials and US drug labels
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
