Ethics and regulatory complexities for pragmatic clinical trials

JAMA

Volumn 311, Issue 23, 2014, Pages 2381-2382

  Sugarman, Jeremy ^a,b   Califf, Robert M ^c  

^a JOHNS HOPKINS UNIVERSITY   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL DECISION MAKING; COMPARATIVE EFFECTIVENESS; DATA PROCESSING; ELECTRONIC MEDICAL RECORD; FOOD AND DRUG ADMINISTRATION; GOVERNMENT REGULATION; HEALTH CARE QUALITY; HUMAN; INFORMED CONSENT; MEDICAL ETHICS; MEDICAL PRACTICE; OUTCOME ASSESSMENT; PATIENT CARE; PATIENT SAFETY; PRIORITY JOURNAL; RANDOMIZED CONTROLLED TRIAL (TOPIC); RISK ASSESSMENT; SAMPLE SIZE; SHORT SURVEY;

COMPARATIVE EFFECTIVENESS RESEARCH; ETHICS COMMITTEES, RESEARCH; EVIDENCE-BASED MEDICINE; GOVERNMENT REGULATION; HUMANS; INFORMED CONSENT; OFF-LABEL USE; PRAGMATIC CLINICAL TRIALS AS TOPIC; RESEARCH SUBJECTS; RISK ASSESSMENT; UNITED STATES; UNITED STATES FOOD AND DRUG ADMINISTRATION;

EID: 84902602802     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2014.4164     Document Type: Short Survey

References (7)

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