Betekenis van:
informed consent

informed consent
Zelfstandig naamwoord
    • consent by a patient to undergo a medical or surgical treatment or to participate in an experiment after the patient understands the risks involved

    Hyperoniemen


    Voorbeeldzinnen

    1. Informed consent applications
    2. The authority responsible for giving consent shall be informed without delay.
    3. Convention on the prior informed consent procedure for certain hazardous chemicals and pesticides in international trade.
    4. that, in the event of sub-processing, it has previously informed the data exporter and obtained its prior written consent;
    5. Secretariat for the Rotterdam Convention on the Prior Informed Consent Procedure for Certain Hazardous Chemicals and Pesticides in International Trade
    6. Before the commencement of any field trial, the informed consent of the owner of the animals to be used in the trial shall be obtained and documented.
    7. on the conclusion, on behalf of the European Community, of the Rotterdam Convention on the Prior Informed Consent Procedure for certain hazardous chemicals and pesticides in international trade
    8. They should notably address the fundamental rights implications of any possible restrictions on informed consent and the publication of research results related to human health.
    9. The detailed rules adopted by Member States pursuant to Article 3(1) of Directive 2001/20/EC, to protect from abuse individuals who are incapable of giving their informed consent should also cover individuals temporarily incapable of giving their informed consent, as in emergency situations.
    10. the competent authority of transit outside the Community shall have 60 days following the date of transmission of its acknowledgement of receipt of the notification in which to request additional information on the notified shipment, to provide, if the country concerned has decided not to require prior written consent and has informed the other Parties thereof in accordance with Article 6(4) of the Basel Convention, tacit consent or to give a written consent with or without conditions; and
    11. pay particular attention to education, training and dissemination of good practices in electronically recording, storing and processing clinical information as well as in gaining informed consent of the patient and lawfully sharing patient’s personal data;
    12. Pursuant to Regulation (EC) No 304/2003, the Commission is to decide on behalf of the Community, whether or not to permit the import into the Community of each chemical subject to the Prior Informed Consent (PIC) procedure.
    13. In the case of radioactive waste and spent fuel leaving the Community, the third country of destination should not only be informed of the shipment, but should also give its consent to it.
    14. The consent holder must maintain regular contact with operators to ensure that they are informed of any changes to current practice which may change the conclusions of the environmental risk assessment.
    15. However, taking into account the consequences of publication, it should take place only where the economic operator or other person has freely given specific and informed written consent thereto.