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Volumn 61, Issue 2, 2006, Pages 251-272
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The food and drug administration's regulation of risk disclosure for implantable cardioverter defibrillators: Has technology outpaced the agency's regulatory framework?
a a
a
NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
DATA BASE;
DEFIBRILLATOR;
FOOD AND DRUG ADMINISTRATION;
HEALTH HAZARD;
HEART ARRHYTHMIA;
HUMAN;
INFORMATION RETRIEVAL;
INFORMATION SERVICE;
LAW;
MATERIALS;
MEDICAL TECHNOLOGY;
PATIENT SAFETY;
POLICY;
POSTMARKETING SURVEILLANCE;
PRACTICE GUIDELINE;
PROSTHESIS FAILURE;
REVIEW;
RISK BENEFIT ANALYSIS;
RISK FACTOR;
RISK MANAGEMENT;
SUDDEN DEATH;
VOLUNTARY REPORTING;
CONSUMER PRODUCT SAFETY;
DEFIBRILLATORS, IMPLANTABLE;
DEVICE APPROVAL;
DISCLOSURE;
EQUIPMENT FAILURE;
EQUIPMENT SAFETY;
HUMANS;
INDUSTRY;
MANDATORY REPORTING;
PRODUCT LABELING;
PRODUCT SURVEILLANCE, POSTMARKETING;
RISK;
UNITED STATES;
UNITED STATES FOOD AND DRUG ADMINISTRATION;
ELEPHANTIDAE;
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EID: 33745597111
PISSN: 1064590X
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (5)
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References (0)
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