Article D533-11
The following are deemed to be professional clients within the meaning of article L. 533-16, for all investment services and all financial instruments:1. a) The credit institutions referred to in arti…
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Showing 3821–3830 of 4107 articles for “Art. 292 B”
The following are deemed to be professional clients within the meaning of article L. 533-16, for all investment services and all financial instruments:1. a) The credit institutions referred to in arti…
The purpose of the Anti-Money Laundering and Combating the Financing of Terrorism (AML/CFT) Policy Board is : 1° To ensure better coordination between government departments and supervisory authoritie…
I. - The declaration submitted to the minister, the chairman of the authority or the director or chief executive of the establishment or public interest grouping shall include the following informatio…
I.-The Agence nationale pour l'amélioration des conditions de travail is administered by a Board of Directors and managed by a Chief Executive Officer. The Board of Directors comprises : 1° Eleven emp…
I.-The managing legal entity responsible for implementing the supported employment scheme complies with a set of specifications defined, for each managing entity, by the regional health agency, in con…
All entries and withdrawals of substances and medicinal products classified as narcotics are recorded by the persons mentioned in article R. 5132-76 in a register or recorded by a specific computer sy…
…rgone a clinical trial on veterinary medicinal products mentioned in V of article L. 234-2 may only be placed on the market if this trial has not been opposed by the Director General of the Agence nat…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
…nded use means the use for which a medical device is intended according to the information provided by the manufacturer in the labelling, the instruction leaflet or promotional material; 2° Placing on…
…part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessment…
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