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Showing 1671–1680 of 13843 articles for “Art. Case C-264/14”
Monitoring self-vaccines for veterinary use consists of the authorisation holder recording the following information in chronological order: 1° The name and address of the owner of the animal or farm…
The CE marking may be affixed to a medical device only if it complies with the essential health and safety requirements referred to in Section 5 of this Chapter and has undergone the certification pro…
Incidents or risks of incidents as defined in Article L. 5212-2 must be reported immediately.
Manufacturers or their agents, importers and distributors shall declare without delay to the Director General of the Agence nationale de sécurité du médicament et des produits de santé any incidents o…
The provisions of articles R. 5211-15, R. 5211-17, R. 5211-19 and R. 5211-20 are applicable to in vitro diagnostic medical devices.
The Director General of the Agence nationale de sécurité du médicament et des produits de santé is appointed for a period of three years, renewable once. He manages the establishment. He performs all…
In order to provide the most appropriate equipment for the needs of the person who is ill or has an incapacity or disability, the service provider and the equipment distributor will ask the prescriber…
In health care institutions, the collection of information concerning nosocomial infections which must be reported in accordance with article R. 1413-79 is organised according to procedures defined by…
Visits are conducted in accordance with professional secrecy. The institution, all the institutions belonging to or associated with the regional hospital grouping or the organisation which is the subj…
The location of the SMURs mentioned in 2° of article R. 6123-1 is determined by the regional health plan and ensures territorial coverage.
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