Managing medical devices within a regulatory framework
Gespeichert in:
Verfasser / Beitragende:
edited by Beth Ann Fiedler
Ort, Verlag, Jahr:
Amsterdam, Cambridge, MA :
Elsevier,
2017
Beschreibung:
1 online resource (xxiv, 356 pages) : illustrations
Format:
Buch (online)
Online Zugang:
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| 264 | 1 | |a Amsterdam |a Cambridge, MA |b Elsevier |c [2017] | |
| 300 | |a 1 online resource (xxiv, 356 pages) |b illustrations | ||
| 336 | |a text |b txt |2 rdacontent/eng | ||
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| 504 | |a Includes bibliographical references and index. | ||
| 506 | |a Lizenzbedingungen können den Zugang einschränken. License restrictions may limit access. | ||
| 650 | 1 | 2 | |a Equipment and Supplies |0 https://id.nlm.nih.gov/mesh/D004864 |
| 650 | 2 | 2 | |a Medical Device Recalls |x standards |0 https://id.nlm.nih.gov/mesh/D057052Q000592 |
| 650 | 2 | 2 | |a Equipment Safety |x standards |0 https://id.nlm.nih.gov/mesh/D004869Q000592 |
| 650 | 2 | 2 | |a Government Regulation |0 https://id.nlm.nih.gov/mesh/D033161 |
| 650 | 2 | 2 | |a Technology Assessment, Biomedical |x trends |0 https://id.nlm.nih.gov/mesh/D013673Q000639 |
| 700 | 1 | |a Fiedler |D Beth Ann |e editor | |
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