Traduction de «consentement écrit » (Français → Anglais) :

A planned shipment subject to the procedure of prior written notification and consent may take place only after the notification and movement documents have been completed pursuant to this Regulation, taking into account Articles 16(a) and 16(b), and during the period of validity of the written or tacit consents of all competent authorities concerned.

(b)the competent authority of dispatch in the Community shall take the decision to consent to the shipment as referred to in Article 9 only after having received written consent from the competent authority of destination and, where appropriate, the tacit or written consent of the competent authority of transit outside the Community, and not earlier than 61 days following the date of transmission of the acknowledgement by the competent authority of transit.

the competent authority of transit to which the OECD Decision does not apply 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

the competent authority of dispatch in the Community shall take the decision to consent to the shipment as referred to in Article 9 only after having received written consent from the competent authority of destination and, where appropriate, the tacit or written consent of the competent authority of transit outside the Community, and not earlier than 61 days following the date of transmission of the acknowledgement by the competent authority of transit.

Because it recognises the importance of this directive, the European Parliament has endeavoured to overcome its differences rather than hold up the legislative process, focusing on the following safety conditions for clinical trials: the written consent of the subjects to the clinical trial, the consent of the guardian or an authority provided for by law and of the treating doctor to the participation of persons with impaired understanding or a mental disorder which prevents them from giving their consent, the criterion being that the expected benefits of the drug being tested must outweigh any side effects. The participation of children ...[+++] in clinical trials must be regulated properly because it is a particularly sensitive issue.

A person having performed euthanasia covered by a written statement wishing to obtain immunity for this act in Member State A could see to it that he or she is prosecuted in Member State B, withholding the fact that the written consent has been obtained.