Industry perspective on FDA regulation of medical devices and the practice of medicine
Technology and Regulatory Affairs, Health Industry Manufacturers Association, Washington, District of Columbia, USA
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| Veröffentlicht in: | The Annals of thoracic surgery 1996, Vol.61 (1), p.485-486 |
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| Format: | Artikel |
| Sprache: | eng |
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| container_end_page | 486 |
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| container_issue | 1 |
| container_start_page | 485 |
| container_title | The Annals of thoracic surgery |
| container_volume | 61 |
| creator | Tandy, Marlene K. |
| description | Technology and Regulatory Affairs, Health Industry Manufacturers Association, Washington, District of Columbia, USA |
| doi_str_mv | 10.1016/0003-4975(95)00989-2 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0003-4975 |
| ispartof | The Annals of thoracic surgery, 1996, Vol.61 (1), p.485-486 |
| issn | 0003-4975 1552-6259 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_77979513 |
| source | MEDLINE; Free E-Journal (出版社公開部分のみ）; ScienceDirect Freedom Collection (Elsevier); Alma/SFX Local Collection |
| subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Device Approval - legislation & jurisprudence Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care Humans Industry Intensive care medicine Medical sciences United States United States Food and Drug Administration |
| title | Industry perspective on FDA regulation of medical devices and the practice of medicine |
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