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Prescriptive authority, as defined in the Minnesota Pharmacy Act (Statute 151.37) and the Prescribing Drugs and Therapeutic Devices Act (Statute 148.235), is the legal authorization to prescribe, procure, sign for, record, administer, and dispense over the counter, legend, and controlled substances, including sample drugs.
150-hour, 300-patient-contact preceptorship supervised by a physician or other practitioner with prescriptive authority. [45] The certification is renewed biennially with completion of twenty hours of Accreditation Council for Pharmacy Education (ACPE) or category I of the American Medical Association (AMA) approved continuing education. [46]
Actions by medical boards and governmental agencies include revocation, suspension or denial of license renewal. Through the FPDC's Disciplinary Alert Service , the FSMB electronically notifies all member boards within 48 hours when any member board reports a disciplinary action against a physician or physician assistant .
The Minnesota Department of Health (MDH) is the state health agency of the State of Minnesota in the United States. [1] The department has four offices in Saint Paul and seven outside of the Twin Cities metropolitan area: Bemidji , Duluth , Fergus Falls , Mankato , Marshall , Rochester , and St. Cloud .
An act relating to retirement; various Minnesota public employee retirement plans; allowing MSRS-General deferred members to vote in board elections; continuing Stevens County Housing and Redevelopment Authority employees in PERA-General; excluding fixed-route bus drivers employed by the St. Cloud Metropolitan Transit Commission from PERA ...
Electronic prescription (e-prescribing or e-Rx) is the computer-based electronic generation, transmission, and filling of a medical prescription, taking the place of paper and faxed prescriptions.
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The National Council for Prescription Drug Programs (NCPDP) is an American nonprofit standards development organization representing most sectors of the U.S. pharmacy services industry. It was founded in 1977 as the extension of a Drug Ad Hoc Committee that made recommendations for the U.S. National Drug Code (NDC).