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  2. Medical privacy - Wikipedia

    en.wikipedia.org/wiki/Medical_privacy

    Medical privacy, or health privacy, is the practice of maintaining the security and confidentiality of patient records. It involves both the conversational discretion ...

  3. Privacy for research participants - Wikipedia

    en.wikipedia.org/wiki/Privacy_for_research...

    Researchers publish data that they get from participants. To preserve participants' privacy, the data goes through a process to de-identify it. The goal of such a process would be to remove protected health information which could be used to connect a study participant to their contribution to a research project so that the participants will not suffer from data re-identification.

  4. Protected health information - Wikipedia

    en.wikipedia.org/wiki/Protected_health_information

    For example, sharing information about someone on the street with an obvious medical condition such as an amputation is not restricted by U.S. law. However, obtaining information about the amputation exclusively from a protected source, such as from an electronic medical record, would breach HIPAA regulations. Business Associates

  5. Information privacy - Wikipedia

    en.wikipedia.org/wiki/Information_privacy

    Information privacy is the relationship between the collection and dissemination of data, technology, the public expectation of privacy, contextual information norms, and the legal and political issues surrounding them. [1] It is also known as data privacy [2] or data protection.

  6. Medical psychology - Wikipedia

    en.wikipedia.org/wiki/Medical_psychology

    A medical psychologist must obtain specific qualification in psychopharmacology to prescribe psychiatric medications and other pharmaceutical drugs. [1] A trained medical psychologist or clinical psychopharmacologist with prescriptive authority is a mid-level provider who prescribes psychotropic medication such as antidepressants for mental health disorders. [2]

  7. Informed consent - Wikipedia

    en.wikipedia.org/wiki/Informed_consent

    As the medical guidelines established in the Nuremberg Code were imported into the ethical guidelines for the social sciences, informed consent became a common part of the research procedure. [34] However, while informed consent is the default in medical settings, it is not always required in the social sciences.

  8. Dying To Be Free - The Huffington Post

    projects.huffingtonpost.com/dying-to-be-free...

    To enter the drug treatment system, such as it is, requires a leap of faith. The system operates largely unmoved by the findings of medical science. Peer-reviewed data and evidence-based practices do not govern how rehabilitation facilities work. There are very few reassuring medical degrees adorning their walls.

  9. Health information technology - Wikipedia

    en.wikipedia.org/wiki/Health_information_technology

    Healthcare information in EMRs are important sources for clinical, research, and policy questions. Health information privacy (HIP) and security has been a big concern for patients and providers. Studies in Europe evaluating electronic health information poses a threat to electronic medical records and exchange of personal information. [6]