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The Office of State Medical Examiners investigates causes of death that may endanger the community and uses this information to keep the public aware and safe. Environmental and Health Services Regulation licenses and regulates health professionals and monitors beach and drinking water quality.
The Federation of State Medical Boards (FSMB) of the United States is a national non-profit organization that represents the 71 state medical and osteopathic boards of the United States and its territories and co-sponsors the United States Medical Licensing Examination. Medical boards license physicians, investigate complaints, discipline those ...
The Executive Office of Health and Human Services is a cabinet-level agency in Rhode Island. [1] The current EOHHS Secretary is Womazetta Jones. EOHHS was created by the Rhode Island General Assembly in 2006 and is codified in Title 42 Chapter 7.2 of the R.I. General Laws. The agency serves as an umbrella organization for Rhode Island's ...
Any provider between the levels of Emergency medical technician and Paramedic is either a form of EMT-Intermediate or an Advanced EMT. The use of the terms "EMT-Intermediate/85" and "EMT-Intermediate/99" denotes use of the NHTSA EMT-Intermediate 1985 curriculum and the EMT-Intermediate 1999 curriculum respectively.
The Rhode Island State Health Laboratory (RISHL) is the public health laboratory of Rhode Island operated by the Rhode Island Department of Health. The laboratory will be transitioning to a new facility in Providence in 2025.
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Medical devices first came under comprehensive regulation with the passage of the Federal Food, Drug, and Cosmetic Act of 1938 (FD&C), [9] which replaced the earlier Pure Food and Drug Act of 1906. The FD&C allowed the FDA to perform factory inspections and prohibited misbranded marketing of cosmetic and therapeutic medical devices. [10]
An investigational device exemption (IDE) allows an investigational device (i.e. a device that is the subject of a clinical study [1]) to be used in order to collect safety and effectiveness data required to support a premarket approval (PMA) application or a premarket notification [510(k)] submission to Food and Drug Administration (FDA). [2]