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Showing 2591–2600 of 52589 articles for “Art. L 441-10 to L 441-16”
The provisions of 1° of article R. 5132-15 do not apply to the medicinal products mentioned in 2° and 3° of article R. 5124-43. However, the words: "Reserved for professional use", surrounded by a col…
The authorisation holder shall inform the Director General of the Agency of the commencement of the activity covered by the authorisation. He shall also inform him of the definitive cessation of this…
In the companies and their establishments mentioned in 1° and 2° of article R. 5142-1, the pharmacist or veterinarian in charge and the delegated pharmacist(s) or veterinarian(s) must have at least tw…
The CE mark is affixed under the responsibility of the manufacturer or his authorised representative. Its form and dimensions are laid down by order of the Minister for Health. The CE marking must be…
In order to comply with the requirements relating to design and manufacture, in vitro diagnostic medical devices are designed, manufactured and packaged in such a way as to meet the following objectiv…
The reports, whether mandatory or optional, provided for in articles R. 5212-14 and R. 5212-15 are made by manufacturers or their representatives, users or third parties who observe or are aware of in…
At the request of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the manufacturer or its authorised representative shall provide any information relat…
Any healthcare professional who, in the course of his duties within a health care establishment, observes one or more cases of nosocomial infections, informs, on the one hand, the practitioner respons…
The agenda for meetings of the National Committee is set by the minister(s) responsible for social action, health and social security.
The interventions of the SMUR and those of the SMUR branches mentioned in article R. 6123-5 are triggered and coordinated by the SAMU. The mobile emergency and resuscitation structure team informs the…
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