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Clinical peer review, also known as medical peer review is the process by which health care professionals, including those in nursing and pharmacy, evaluate each other's clinical performance. [1] [2] A discipline-specific process may be referenced accordingly (e.g., physician peer review, nursing peer review).
NPACE held its first national conference in Boston in 1992, with one thousand Nurse Practitioners from all over the country in attendance. NPACE began to expand its offerings to other geographic locations. Orlando, Florida became a regular venue for an annual National Primary Care Conference, followed by the Midwest, typically Chicago.
The CPEP approach to physician competency evaluation and assessment has three major components: clinical competence assessment, educational intervention, and post-educational evaluation. [citation needed] The assessment is individualized based on the physician’s practice and the concerns of the referring organization. [4]
The objectives of a well-run M&M conference are to identify adverse outcomes associated with medical error, to modify behavior and judgment based on previous experiences, and to prevent repetition of errors leading to complications. [2] Conferences are non-punitive and focus on the goal of improved patient care.
Based on an evaluation of the potential safety concern, The FDA may take regulatory action(s) to improve product safety and protect the public health, such as updating a product's labeling information, restricting the use of the drug, communicating new safety information to the public, or, in rare cases, removing a product from the market.
Further, since peer review activity is commonly segmented by clinical discipline, there is also physician peer review, nursing peer review, dentistry peer review, etc. [11] Many other professional fields have some level of peer review process: accounting, [12] law, [13] [14] engineering (e.g., software peer review, technical peer review ...
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A sponsor sends a feasibility questionnaire to the local research site. The Clinical Research Coordinator completes the form on behalf of the site to determine if the local site has the patient population, support staff, medical facilities, and equipment necessary to successfully carry out the study protocol.