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Showing 6751–6760 of 43956 articles for “Art. L. 145-5”
…case, the foreseeable risk and the constraints involved in the clinical investigation must be minimal.
…tion from the duly informed data subjects, to the individual data strictly necessary for this control. They are subject to professional secrecy under the conditions defined by articles 226-13 and 226-…
…gulation (EU) No 2017/745 of the European Parliament and of the Council of 5 April 2017 and Article L. 1121-6, is punishable by three years' imprisonment and a fine of €45,000.
…rior to its implementation and, in the case of clinical investigations referred to in II of Article L. 1125-1, authorisation from the competent authority in accordance with the provisions of this same…
No clinical investigation may be carried out on a person without his free and informed consent, obtained in writing under the conditions laid down in paragraph 1 of Article 63 of Regulation (EU) 2017/…
…aving the necessary competence to examine the project, under the conditions provided for in Article L. 1123-14 or Article L. 1123-16. It may only request one opinion per clinical investigation project…
At the time of giving informed consent, the investigator may ask the person undergoing clinical investigation to agree to his/her data being used in subsequent research for scientific purposes only. T…
…of the Council of 5 April 2017; 2° The conditions applicable to the appeals provided for in Article L. 1125-4; 3° The minimum guarantees for the insurance provided for in the third paragraph of Articl…
In order to implement an employee's entitlement to the leave referred to in Article L. 3142-60, a company collective agreement or agreement or, failing that, a branch agreement or agreement shall dete…
…cated in the right-hand column of the same table: Articles applicable In the wording resulting from L. 544-2 Law no. 2003-706 of 1 August 2003 L. 544-3 to L. 544-6 Law no. 2019-486 of 22 May 2019
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