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The two main reference sources providing this information are the British National Formulary (BNF) and the Drug Tariff. There is a section in the Drug Tariff, known unofficially as the " Blacklist ", detailing medicines which are not to be prescribed under the NHS and must be paid for privately by the patient.
The British National Formulary (BNF) is a United Kingdom (UK) pharmaceutical reference book that contains a wide spectrum of information and advice on prescribing and pharmacology, along with specific facts and details about many medicines available on the UK National Health Service (NHS). Information within the BNF includes indication(s ...
National Institute for Biological Standards and Control – responsible for the standardisation and control of biological medicines; The MHRA has several independent advisory committees which provide the UK Government with information and guidance on the regulation of medicines and medical devices.
Pharmaceutical policy is a branch of health policy that deals with the development, provision and use of medications within a health care system.It embraces drugs (both brand name and generic), biologics (products derived from living sources, as opposed to chemical compositions), vaccines and natural health products.
National Cancer Institute NCTMB: Nationally certified in therapeutic massage and bodywork NEJM: New England Journal of Medicine: NHC: Nephrology Hypertension Clinic, P.C: NHS: National Health Service: NICE: National Institute for Health and Clinical Excellence: NKC: Northwest Kidney Centers: NKF: National Kidney Foundation: NYHA: New York Heart ...
Together with the British National Formulary (BNF), the British Pharmacopoeia defines the UK's pharmaceutical standards. Pharmacopoeial standards are compliance requirements; that is, they provide the means for an independent judgement as to the overall quality of an article, and apply throughout the shelf-life of a product.
Providing information on formulary or tiered formulary medications, patient eligibility, and authorization requirements received electronically from the patient's insurance provider System integration capabilities (e.g., connection with various databases, connection with pharmacy and pharmacy benefit manager systems)
USP establishes documentary (written) and reference (physical) standards for medicines, food ingredients, dietary supplement products, and ingredients. These standards are used by regulatory agencies and manufacturers to help to ensure that these products are of the appropriate identity, as well as strength, quality, purity, and consistency.