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CONSENT STATEMENT OF PATIENT

См. также в других словарях:

  • patient's bill of rights — A general statement of patient rights voluntarily adopted by most health care providers, covering matters such as access to care, patient dignity and confidentiality, personal safety, consent to treatment and explanation of charges. Similar… …   Black's law dictionary

  • patient’s bill of rights — n. A statement of patients’ rights adopted by many hospitals and health care providers, and made law by the federal government and several states, that covers topics such as confidentiality, consent to treatment, and dignity. The Essential Law… …   Law dictionary

  • Patient Information Advisory Group — The Patient Information Advisory Group (PIAG) was established in the United Kingdom under section 61 [ [http://www.opsi.gov.uk/acts/acts2001/10015 g.htm#61 section 61 of the Health and Social Care Act 2001] ] of the Health and Social Care Act… …   Wikipedia

  • MEDICINE AND LAW — This article is arranged according to the following outline: introduction Judicial Decision – A Value Determination the values of a jewish and democratic state in the image of god PHYSICIAN S DUTIES AND PATIENTS RIGHTS the physician and the judge …   Encyclopedia of Judaism

  • Electroconvulsive therapy — Intervention ICD 10 PCS GZB ICD 9 CM 94.27 …   Wikipedia

  • Socialized medicine — is a term used to describe a system for providing medical and hospital care for all at a nominal cost by means of government regulation of health services and subsidies derived from taxation.[1] It is used primarily and usually pejoratively in… …   Wikipedia

  • Сас, Томас — Томас Сас Thomas Stephen Szasz Дата рождения: 15 апреля 1920(1920 04 15) Место рождения: Будапешт, Венгрия Дата смерти …   Википедия

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  • Paraphilia — Classification and external resources MeSH D010262 Paraphilia (in Greek para παρά = beside and philia φιλία = friendship, having the meaning of love) is a biomedical term used to describe sexual arousal to objects, situations, or indi …   Wikipedia

  • Clinical research coordinator — The Clinical Research Coordinator (CRC) is responsible for conducting clinical trials using good clinical practice [1] (GCP) under the auspices of the Principal Investigator (PI). Good Clinical Practices Principles have been defined by Madelene… …   Wikipedia

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