Примери за използване на Designated representative на Английски и техните преводи на Български
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Designated representative of that person.
The informed consent of their legally designated representative has been obtained;
The EDPB designated representatives for the third annual review of the Privacy Shield.
(a) enable the subject or his or her legally designated representative to understand.
Apart from the designated representative, is there anyone else who can influence respondent to accept the outcome of the negotiation?
What is the likely negotiation approach of the designated representative from the other party?
The designated representatives shall, within 2(two) business days after being designated, confer by telephone or in person to attempt to resolve the dispute.
Such permit may be revoked at any time by the County or its designated representative.
We were watching our designated representatives(police, FBI) doing their job in front of us.
That consent may be withdrawn at any time by the subject or his or her legally designated representative.
Adequate time shall be given for the subject or his or her legally designated representative to consider his or her decision to participate in the clinical trial.
The Security Council shall hold periodic meetings at which each of itsmembers may, if it so desires, be represented by a member of thegovernment orby some other specially designated representative.
Of the identifying details of the owner,of the persons responsible and the designated representative in accordance with art. 5, section 2;
The information referred to in paragraph 2 shall be prepared in writing and be available to the subject or, where the subject is not able to give informed consent,his or her legally designated representative.
Its development required the establishment of an interinstitutional steering committee, which designated representatives for each institution and for each language.
If the subject or, where applicable,his or her legally designated representative does not give consent, he or she shall be informed of the right to object to the use of data obtained from the clinical trial.
Member States shall ensure effective, efficient andsecure cooperation of the designated representatives in the Cooperation Group.
The subject or, where the subject is not able to give informed consent,his or her legally designated representative shall be provided with a copy of the document or the record, as appropriate, by which informed consent has been given.
Informed consent shall be written, dated and signed by the person performing the interview referred to in point(c) of paragraph 2, and by the subject or, where the subject is not able to give informed consent,his or her legally designated representative after having been duly informed in accordance with paragraph 2.
(g) the subject or, where the subject is not able to give informed consent,his or her legally designated representative, has been provided with the contact details of an entity where further information can be received in case of need;
Informed consent' means a subject's free and voluntary expression of his or her willingness to participate in a particular clinical investigation, after having been informed of all aspects of the clinical investigation that are relevant to the subject's decision to participate or, in the case of minors and of incapacitated subjects, an authorisation oragreement from their legally designated representative to include them in the clinical investigation;
The subject or, where the subject is not ableto give informed consent, his or her legally designated representative has given informed consent, in accordance with Article 59;
For the purposes of point(b),where informed consent has been obtained from the legally designated representative, informed consent to continue the participation in the clinical trial shall be obtained from the subject as soon as he or she is capable of giving informed consent.
In the case of clinical trials in emergency situations as referredto in Article 35, the procedure for obtaining the informed consent of the subject or the legally designated representative to continue the clinical trial shall be described;
Without prejudice to Directive 95/46/EC, the sponsor may ask the subject or, where the subject is not able to give informed consent, his orher legally designated representative at the time when the subject or the legally designated representative gives his or her informed consent to participate in the clinical trial to consent to the use of his or her data outside the protocol of the clinical trial exclusively for scientific purposes.
The performance study relates directly to the subject's medical condition because of which it is not possible within the therapeutic window to obtain prior informed consent from the subject or from his or her legally designated representative and to supply prior information, and the performance study is of such a nature that it may be conducted exclusively in emergency situations;
(e) documents which relate to any changes to the information provided to subjects or their legally designated representatives, the informed consent procedure, informed consent forms, information sheets, or to letters of invitation; and.
The subjects, or where a subject is not able to give informed consent,his or her legally designated representative, have been informed in accordance with Article 29(2) to(6);
In addition to any consultation with referring DPAs on case-specific matters,the FTC commits to participate in periodic meetings with designated representatives of the Article 29 Working Party to discuss in general terms how to improve enforcement cooperation with respect to the Framework.
This Regulation is without prejudice to national law requiring that,in addition to the informed consent given by the legally designated representative, a minor who is capable of forming an opinion and assessing the information given to him or her, shall also assent in order to participate in a clinical investigation.