Article R7124-1
…e L. 7124-1 must first submit an application for authorisation to the Prefect of the company's registered office. If the registered office of the company is abroad or if the company has no fixed regis…
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Showing 8961–8970 of 69883 articles for “Art. I-1°-a ter”
…e L. 7124-1 must first submit an application for authorisation to the Prefect of the company's registered office. If the registered office of the company is abroad or if the company has no fixed regis…
…spection officer observes one of the breaches of the obligations mentioned in section 2 of this chapter, he sends the Regional Director of Companies, Competition, Consumption, Labour and Employment a…
The public health inspecting pharmacists carry out inspections of the pharmacies and dispensaries mentioned in articles L. 5125-1, L. 5125-19, L. 5126-1, L. 5126-8, L. 5126-9 and L. 5126-13, places wh…
The extemporaneous preparation of veterinary medicinal products, including the extemporaneous preparation of medicated feed provided for in article L. 5143-3, is carried out in accordance with good pr…
The Director of the National Veterinary Medicines Agency is appointed by order of the Ministers for Agriculture and Health, on a proposal from the Director General of the National Agency for Food, Env…
The provisions of articles R. 5211-25 to R. 5211-29 are applicable to in vitro diagnostic medical devices.
…ulated health product which, under these regulations, bears the CE mark";h) Where applicable, the internal reference number;3° Does not include a statement to the effect that the medical device is rei…
The purpose of materiovigilance is to monitor incidents or risks of incidents resulting from the use of medical devices which are defined in article L. 5211-1 and come under this title by virtue of ar…
…defined in 1° of article R. 5222-2. It is carried out on all in vitro diagnostic medical devices after they have been placed on the market, as well as on the in vitro diagnostic medical devices menti…
…lated health product which, under these regulations, bears the CE mark"; h) Where applicable, the internal reference number; 3° Does not include any statement to the effect that the in vitro diagnosti…
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