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write (write on the label) s.a. secundum artem: according to the art (accepted practice or best practice) SC subcutaneous "SC" can be mistaken for "SL," meaning sublingual. See also SQ: sem. semen seed s.i.d. semel in die: once a day used exclusively in veterinary medicine sig. signa, signetur: write (write on the label) s̄ sine
A drug label retrieved from a random clinic in Hong Kong. Over-prominence of the logo of clinics may be susceptible to the poor interpretation of drugs by patients. An effective drug label should demonstrate efficacy and safety. Imperfect drug label information or design may lead to misinterpretation and hence medication errors.
The Joint Commission is a United States-based nonprofit tax-exempt 501(c) organization [1] that accredits more than 22,000 US health care organizations and programs. [2] The international branch accredits medical services from around the world.
The Prescribing Information follows one of two formats: "physician labeling rule" format or "old" (non-PLR) format. For "old" format labeling a "product title" may be listed first and may include the proprietary name (if any), the nonproprietary name, dosage form(s), and other information about the product. The other sections are as follows:
Founded in 1951, the Joint Commission (TJC, previously abbreviated as JCAHO) is an independent, not-for-profit organization that evaluates and accredits nearly 15,000 healthcare organizations and programs in the United States. An organization must undergo an on-site survey by a Joint Commission survey team at least every three years.
Bar code medication administration (BCMA) is a barcode system designed by Glenna Sue Kinnick to prevent medication errors in healthcare settings and to improve the quality and safety of medication administration. The overall goals of BCMA are to improve accuracy, prevent errors, and generate online records of medication administration.
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The national drug code is a unique 10 or 11 digit, 3-segment numeric identifier assigned to each medication listed under Section 510 of the US Federal Food, Drug, and Cosmetic Act. The segments identify the labeler or vendor , product (within the scope of the labeler), and trade package (of this product).
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