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Volumn 9, Issue 1, 2008, Pages 67-68
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Clarification of FDA and the joint commission reporting requirements for US tissue recipient adverse reactions
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Author keywords
[No Author keywords available]
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Indexed keywords
ACCESS TO INFORMATION;
BACTERIAL INFECTION;
COMMUNICABLE DISEASE;
DISEASE TRANSMISSION;
FOOD AND DRUG ADMINISTRATION;
GOOD CLINICAL PRACTICE;
GRAFT RECIPIENT;
HEALTH CARE FACILITY;
HEALTH CARE ORGANIZATION;
HUMAN;
INFORMATION PROCESSING;
LETTER;
MANDATORY REPORTING;
PATIENT SAFETY;
PRIORITY JOURNAL;
QUALITY CONTROL;
TISSUE TRANSPLANTATION;
UNITED STATES;
BACTERIAL INFECTIONS;
COMMUNICABLE DISEASE CONTROL;
HUMANS;
TISSUE TRANSPLANTATION;
UNITED STATES;
UNITED STATES FOOD AND DRUG ADMINISTRATION;
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EID: 39549105598
PISSN: 13899333
EISSN: None
Source Type: Journal
DOI: 10.1007/s10561-007-9043-2 Document Type: Letter |
Times cited : (2)
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References (1)
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