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Showing 1441–1450 of 15706 articles for “Art. CE 16-7-2021 n° 448500”
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…
…and the delegated pharmacist(s) or veterinarian(s) must have at least two years' practical experience in one or more establishments authorised to manufacture or import veterinary medicinal products i…
…r third parties who observe or are aware of incidents or risks of incidents involving a medical device. Third parties are considered to be persons who are neither manufacturers or their agents or user…
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…
The list of decisions of the Director General referred to in Article L. 5322-2 which are communicated to the Ministers for the Economy, Health and Social Security for information fifteen days before t…
The purpose of the vigilance exercised over the software mentioned in 18° of Article L. 5311-1 and the devices mentioned in 19° of the same article, used in medical biology laboratories, is to monitor…
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…
The contract sets out the procedures for evaluating the implementation of the objectives and commitments, and in particular provides for the indicators required for this evaluation.The results of this…
The provisions of Article R. 6123-161 and those of 2° of Article R. 6123-162 do not apply to the heavy equipment mentioned in Article L. 6122-14-1.
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