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  2. Informed consent - Wikipedia

    en.wikipedia.org/wiki/Informed_consent

    Informed consent is a principle in medical ethics, medical law, media studies, and other fields, that a person must have sufficient information and understanding before making decisions about accepting risk, such as their medical care. Pertinent information may include risks and benefits of treatments, alternative treatments, the patient's role ...

  3. Rotterdam Convention - Wikipedia

    en.wikipedia.org/wiki/Rotterdam_Convention

    t. e. The Rotterdam Convention (formally, the Rotterdam Convention on the Prior Informed Consent Procedure for Certain Hazardous Chemicals and Pesticides in International Trade) is a multilateral treaty to promote shared responsibilities in relation to importation of hazardous chemicals. The convention promotes open exchange of information and ...

  4. Free, prior and informed consent - Wikipedia

    en.wikipedia.org/wiki/Free,_prior_and_informed...

    Free, prior and informed consent ( FPIC) is aimed to establish bottom-up participation and consultation of an indigenous population prior to the beginning of development on ancestral land or using resources in an indigenous population's territory. [ 1] Indigenous people have a special connection to their land [citation needed] and resources ...

  5. Informed Consent in Medical Research - Wikipedia

    en.wikipedia.org/wiki/Informed_Consent_in...

    978-0-727-91486-6. Informed Consent in Medical Research is a medical textbook on medical ethics, authored by Jeffrey S. Tobias and Len Doyal, and published by Wiley in 2001. It was produced in response to the debates between the authors in 1997, following the response to the 1990's British Medical Journal publications of studies in which ...

  6. Dynamic consent - Wikipedia

    en.wikipedia.org/wiki/Dynamic_consent

    Dynamic consent is an approach to informed consent that enables on-going engagement and communication between individuals and the users and custodians of their data. It is designed to address the many issues that are raised by the use of digital technologies in research and clinical care that enable the wide-scale use, linkage, analysis and integration of diverse datasets and the use of AI and ...

  7. Informed assent - Wikipedia

    en.wikipedia.org/wiki/Informed_assent

    Informed assent. The term informed assent describes the process whereby minors may agree to participate in clinical trials. It is similar to the process of informed consent in adults, however there remains some overlap between the terms. [citation needed]

  8. Consent search - Wikipedia

    en.wikipedia.org/wiki/Consent_search

    Consent search. Consent searches (or consensual searches) are searches conducted by United States law enforcement after obtaining the voluntary consent of the person being investigated. In some cases, consent may also be obtained from certain third-parties. [1] Searches that are the product of consent are one of several recognized exceptions to ...

  9. Informed refusal - Wikipedia

    en.wikipedia.org/wiki/Informed_refusal

    Informed refusal. Informed refusal is where a person has refused a recommended medical treatment based upon an understanding of the facts and implications of not following the treatment. [1] [2] Informed refusal is linked to the informed consent process, as a patient has a right to consent, but also may choose to refuse.

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