Workplace Safety » Medical Devices
The following are related categories found throughout the Libraries and Directories. Please click on the category to visit that category - a new browser window will open. Each library requires a seperate subscription.
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Law and the physician, medicine and law, medical liability, etc. Resources, cases, statutes, memos and articles on health law. Latex allergy litigation.
- Medicine / Radiation : Resources related to nuclear medicine
Emphasis on safety & health references for the nuclear medicine department.
- Risk Mgt / Medical Liability : Medical malpractice, risk management in medicine, insurance, etc.
Medical professional liability exposures. Tips to prevent malpractice claims. Handbook on risk management for physicians. State-specific legislative information. Series of risk management forms and letters available for download. Answers to common questions about the release of medical records. Emergency room risk management. Series of articles on risk management and medical professional liability.
- Safety / Medical Devices : FDA regulatory guidance for manufacturers of medical devices
US Food and Drug Administration guidance on the CDRH requirements related to medical device manufacturing safety requirements - recalls, reporting, quality, use errors, etc. Various inspection guides used by FDA field staff for audits. Mammography facility regulatory guidance.
- Safety / Needlesticks : Needlestick injury prevention, legislation, safety devices
Resource materials related to needlestick injury prevention, safety statistics, state laws, federal legislation, safety devices, safety training, etc.
- Safety / Patient Safety : Medical errors, medication errors, patient safety guidance
JCAHO Sentinel Events. Medication Error Prevention Programs. Medical Error Reporting. Guidance regarding patient safety.
- USA Government / FDA : Departments and agencies of US Food and Drug Administration
Departments and agencies of US Food and Drug Administration
- Health Care Safety / Medical Devices : FDA regulatory guidance for manufacturers of medical devices
US Food and Drug Administration guidance on the CDRH requirements related to medical device manufacturing safety requirements - recalls, reporting, quality, use errors, etc. Various inspection guides used by FDA field staff for audits. Mammography facility regulatory guidance.
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