Article R761-5
For the application of this book in Mayotte: 1° References to the departmental prefect are replaced by references to the representative of the State; 2° References to the Court of Appeal are replaced…
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Showing 3821–3830 of 55685 articles for “Art. Cass. soc. 5 November 1987 · Cass. soc. 2 April 1998 · Cass. soc. 2 July 1981 · Cass. soc. 5 November 2009 · Cass. soc. 29 June 2017 · Cass. soc. 28 September 2010 · Cass. soc. 24 October 1989 · CA Paris 16 December 2009”
For the application of this book in Mayotte: 1° References to the departmental prefect are replaced by references to the representative of the State; 2° References to the Court of Appeal are replaced…
It is punishable by one year's imprisonment and a fine of 15,000 euros to carry out or cause to be carried out research involving the human person: 1° Without having obtained a favourable opinion from…
…opportunity to present his observations, provided that one of the conditions set out in articles R. 53-1 and R. 53-2 ceases to be fulfilled or the ad hoc administrator has not complied with the obliga…
…s from the national committee for prevention and health at work, and monitors their implementation; 2° Examines the annual report on working conditions drawn up by the departments of the Ministry resp…
In the case of training courses involving a distance from the trainee's usual place of residence, the trainees concerned are entitled, in order to enable them to return periodically, to reimbursement…
…he commission, after receiving a referral from the administrative authority defined in article R. 7124-1, proposes to the latter, after the employer concerned has been given the opportunity to present…
The provisions of article L. 214-24-28 shall apply to AIFs covered by this paragraph.
For all research involving humans, the sponsor must pass on to the investigators concerned any information likely to affect the safety of individuals.
…tigator(s). These records shall be transmitted to the competent authority mentioned in Article L. 1123-12, at its request.
For the research referred to in 1° of Article L. 1121-1 involving labile blood products, the sponsor shall report to the Agence nationale de sécurité du médicament et des produits de santé any adverse…
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