Article R561-12
For the application of Article L. 561-5-1, the persons mentioned in Article L. 561-2 shall: 1° Before entering into a business relationship, collect and analyse the information necessary to understand…
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Showing 7101–7110 of 17798 articles for “Art. 5°”
For the application of Article L. 561-5-1, the persons mentioned in Article L. 561-2 shall: 1° Before entering into a business relationship, collect and analyse the information necessary to understand…
…do not involve a transfer or direct debit to and from a payment account identified by a RIB or IBAN;5° Money transmission transactions, as defined in Article L. 314-1;6° Electronic money payment trans…
…for risk management and the efficiency of the healthcare system referred to in article R. 1434-19; 5° Giving an opinion on the draft regional multi-year action plan to improve the appropriateness of…
The provision of prior information and the collection in writing of the free and informed consent of each of the members of the couple or of the unmarried woman provided for in the last paragraph of A…
…shoes and boots, umbrellas; b) Moisture, water, such as washing-up gloves; c) Heat, such as gloves; 5° Helmets and visors intended for users of two- or three-wheeled motor vehicles; 6° Personal protec…
…surgeons ; 3° The professional section for midwives ; 4° The professional section for pharmacists; 5° The professional section of medical biologists; 6° The professional section of nurses; 7° The pro…
Contracts may be awarded in separate lots, unless their subject does not allow separate services to be identified. The National Council determines the number, size and purpose of the lots. It may limi…
The deliberations of the National Committee, listed in article R. 4643-5, are automatically enforceable, with the exception of those concerning the vote on the budget. The latter are adopted and made…
No medical device may be placed on the market or put into service in France unless it complies with the essential health and safety requirements referred to in section 5 of this chapter which apply to…
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the in vitro diagnostic medical device with…
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