Article L214-144
The subscription and acquisition of units or shares in a general-purpose professional fund are reserved for professional clients as referred to in article L. 533-16 and for foreign investors belonging…
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Showing 2031–2040 of 65306 articles for “Art. L 642-1 to L 642-19”
The subscription and acquisition of units or shares in a general-purpose professional fund are reserved for professional clients as referred to in article L. 533-16 and for foreign investors belonging…
The general regulations of the Autorité des marchés financiers shall set the conditions for the subscription, sale and redemption of units or shares issued by such an AIF.By way of derogation from the…
When a general-purpose professional fund is a master AIF, the rules governing investment holding, canvassing and marketing of the feeder AIF are those of the master AIF.
Any foreign national wishing to enter France with a view to staying for a period not exceeding three months must apply to the French diplomatic and consular authorities for a short-stay visa, under th…
All employers are required to promote the employment of disabled workers. To this end, employers must declare the total number of beneficiaries of the employment obligation mentioned in article L. 521…
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…
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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