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Volumn , Issue , 2006, Pages 5675-5678
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A medical device regulatory framework case study: South Africa
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Author keywords
[No Author keywords available]
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Indexed keywords
BENCHMARKING;
HEALTH CARE;
MATHEMATICAL MODELS;
REGULATORY COMPLIANCE;
STANDARDIZATION;
COMPACT MODELS;
GLOBAL STANDARDIZATION;
HARMONIZATION;
INTEGRATED REGULATORY FRAMEWORKS;
BIOMEDICAL EQUIPMENT;
ARTICLE;
DEVICE APPROVAL;
DEVICE SAFETY;
DEVICES;
EQUIPMENT DESIGN;
EVIDENCE BASED MEDICINE;
HEALTH;
HUMAN;
MEDICAL DEVICE;
NONBIOLOGICAL MODEL;
POSTMARKETING SURVEILLANCE;
SOUTH AFRICA;
STANDARD;
DEVICE APPROVAL;
DURABLE MEDICAL EQUIPMENT;
EQUIPMENT AND SUPPLIES;
EQUIPMENT DESIGN;
EQUIPMENT SAFETY;
EVIDENCE-BASED MEDICINE;
HUMANS;
MODELS, ORGANIZATIONAL;
PRODUCT SURVEILLANCE, POSTMARKETING;
SOUTH AFRICA;
WORLD HEALTH;
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EID: 34047155007
PISSN: 05891019
EISSN: None
Source Type: Conference Proceeding
DOI: 10.1109/IEMBS.2006.259647 Document Type: Conference Paper |
Times cited : (3)
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References (11)
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