01821nam 2200433Ia 450 991069881070332120090603155720.0(CKB)5470000002397763(OCoLC)369319736(EXLCZ)99547000000239776320090603d2006 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierGuidance for industry[electronic resource] patient-reported outcome measures, use in medical product development to support labeling claimsRockville, MD :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research :Center for Biologics Evaluation and Research :Center for Devices and Radiological Health,[2006]ii, 32 pages digital, PDF fileTitle from PDF title page (viewed on June 3, 2009)."Draft guidance"."Clinical/medical"."February 2006".Guidance for industry Outcome assessment (Medical care)United StatesMedical instruments and apparatusLabelingGovernment policyUnited StatesDrugsLabelingGovernment policyUnited StatesOutcome assessment (Medical care)Medical instruments and apparatusLabelingGovernment policyDrugsLabelingGovernment policyCenter for Drug Evaluation and Research (U.S.)Center for Biologics Evaluation and Research (U.S.)Center for Devices and Radiological Health (U.S.)GPOGPOBOOK9910698810703321Guidance for industry3434577UNINA