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Showing 1101–1110 of 3137 articles for “Art. 18 févr. 1998”
The label of magistral or officinal preparations intended for veterinary medicine covered by the regulations of this section must include the following information: 1° Name and address of the pharmaci…
The establishment in which the operations for which authorisation has been granted are carried out operates in compliance with the rules of good practice laid down under the conditions referred to in…
By way of derogation from the first paragraph of Article R. 5141-16, for the veterinary medicinal products mentioned in this Article, the dossier attached to the marketing authorisation application is…
The pharmacist or veterinary surgeon in charge of the companies mentioned in 4°, 5°, 6°, 7°, 8°, 9° and 10° of article R. 5142-1 and the pharmacist(s) or veterinary surgeon(s) in charge of their estab…
Medical devices which comply with the standards applicable to them, transposing the harmonised European standards, the references of which have been published in the Journal officiel de la République…
The provisions of articles R. 5211-25 to R. 5211-29 are applicable to in vitro diagnostic medical devices.
For a new device, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, at any time and for a period of two years following the declaration provided for…
The Board comprises : 1° Ten members, appointed for a renewable period of three years by order of the Minister for Health on the basis of their scientific expertise in the field of health products, on…
The provisions of this section apply to health care organisations with an in-house pharmacy and to health cooperation groups managing an in-house pharmacy which provide their own sterilisation of medi…
Any establishment authorised to carry out the activity referred to in 3° of article R. 6123-1 is obliged to admit to its emergency department on a permanent basis any person presenting in an emergency…
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