Adverse event reporting for medical devices.
(eBook)
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Citations
United States. Department of Health and Human Services. Office of Inspector General. (2009). Adverse event reporting for medical devices . Department of Health and Human Services, Office of Inspector General.
Chicago / Turabian - Author Date Citation, 17th Edition (style guide)United States. Department of Health and Human Services. Office of Inspector General. 2009. Adverse Event Reporting for Medical Devices. Department of Health and Human Services, Office of Inspector General.
Chicago / Turabian - Humanities (Notes and Bibliography) Citation, 17th Edition (style guide)United States. Department of Health and Human Services. Office of Inspector General. Adverse Event Reporting for Medical Devices Department of Health and Human Services, Office of Inspector General, 2009.
MLA Citation, 9th Edition (style guide)United States. Department of Health and Human Services. Office of Inspector General. Adverse Event Reporting for Medical Devices Department of Health and Human Services, Office of Inspector General, 2009.
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Grouping Information
| Grouped Work ID | 926c5627-3105-5e91-aac7-0b9dfb4ab958-eng |
|---|---|
| Full title | adverse event reporting for medical devices |
| Author | united states department of health and human servi |
| Grouping Category | book |
| Last Update | 2022-07-13 05:41:45AM |
| Last Indexed | 2024-06-26 00:15:04AM |
Book Cover Information
| Image Source | default |
|---|---|
| First Loaded | Jan 10, 2023 |
| Last Used | Jan 19, 2024 |
Marc Record
| First Detected | Oct 31, 2016 12:00:00 AM |
|---|---|
| Last File Modification Time | Aug 18, 2021 03:33:11 AM |
MARC Record
| LEADER | 01532nam a2200385 i 4500 | ||
|---|---|---|---|
| 001 | ocn961477237 | ||
| 003 | OCoLC | ||
| 005 | 20161031105930.0 | ||
| 006 | m o d f | ||
| 007 | cr mn||||||||| | ||
| 008 | 161031s2009 mdua ob f000 0 eng c | ||
| 040 | |a GPO|b eng|e rda|e pn|c GPO | ||
| 042 | |a pcc | ||
| 043 | |a n-us--- | ||
| 074 | |a 0445-B-07 (online) | ||
| 086 | 0 | |a HE 1.75:OEI-01-08-00110 | |
| 088 | |a OEI-01-08-00110 | ||
| 099 | |a HE 1.75:OEI-01-08-00110 | ||
| 110 | 1 | |a United States.|b Department of Health and Human Services.|b Office of Inspector General,|e author. | |
| 245 | 1 | 0 | |a Adverse event reporting for medical devices. |
| 246 | 1 | |i Running title:|a Adverse event reporting for medical devices. | |
| 264 | 1 | |a [Washington, D.C.] :|b Department of Health and Human Services, Office of Inspector General,|c 2009. | |
| 300 | |a 1 online resource (iv, 29 pages) :|b illustrations. | ||
| 336 | |a text|2 rdacontent. | ||
| 337 | |a computer|2 rdamedia. | ||
| 338 | |a online resource|2 rdacarrier. | ||
| 500 | |a "October 2009." | ||
| 500 | |a "OEI-01-08-00110." | ||
| 500 | |a CRDP Project record. | ||
| 504 | |a Includes bibliographical references. | ||
| 588 | |a Description based on online resource; title from PDF title page (HHS, viewed Oct. 28, 2016) | ||
| 610 | 2 | 0 | |a Center for Devices and Radiological Health (U.S.) |
| 650 | 0 | |a Products liability|x Medical instruments and apparatus|x Reporting|z United States. | |
| 650 | 0 | |a Consumer protection|z United States. | |
| 856 | 4 | 0 | |u http://purl.fdlp.gov/GPO/gpo73890|z Online Version |