Article R5121-29-1
When an application for authorisation concerns a generic medicinal product of a reference medicinal product which has not been authorised in France, the applicant must indicate the Member State of the…
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Showing 6731–6740 of 59430 articles for “Art. Cass. 1ère civ. 5-1-2023”
When an application for authorisation concerns a generic medicinal product of a reference medicinal product which has not been authorised in France, the applicant must indicate the Member State of the…
Candidates who obtain an average of 10 out of 20 or more in all the tests defined in article A. 212-120 are offered final admission to the examination for the common part of the third-degree state dip…
Candidates for the examination for the common part of the third-degree state diploma in sports education must pass tests relating to the knowledge programme set out in annex II-8 to this code. This ex…
Article L. 22-10-36 of the French Commercial Code applies to the insurance and reinsurance companies referred to in Articles L. 310-1 and L. 310-1-1 which take the form of a société anonyme and whose…
Before a clinical investigation is carried out, information is given to the person taking part by the investigator or by a doctor representing him. Where the investigator is a qualified person, this i…
Clinical investigations may only be carried out in a place that has the human, material and technical resources appropriate to the clinical investigation and compatible with the safety requirements of…
I.-For the duration of the clinical investigation involving an intervention on the patient which is not justified by the patient's usual care and which exposes the patient to risks and constraints whi…
I.-The Data Protection Committee gives its opinion on the conditions for the validity of the clinical investigation, particularly with regard to :the protection of individuals, in particular the prote…
The clinical investigation does not give rise to any direct or indirect financial compensation for the persons who take part in it, apart from the reimbursement of expenses incurred and, where applica…
I.-The clinical investigations of the devices mentioned in Article 1 of Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 are governed by the provisions of the afo…
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