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Showing 4261–4270 of 52309 articles for “Art. Cass. ass. plén. 2-10-2015 n° 14-14.256”
I. - Authorisation is issued to a natural person for all or part of a strain of micro-organism or a type of toxin and for one or more of the operations mentioned in the first paragraph of Article R. 5…
Persons manufacturing or marketing the substances, plants, medicinal products and other products mentioned in article R. 5132-98 shall, at their request, provide the Director General of the Agence nat…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé provides all relevant information to the European Medicines Agency, as well as to the International Narc…
The drug dependence and addictovigilance assessment and information centres carry out their vigilance missions relating to health products under the conditions defined in article R. 1413-61-4.
…rule which applies shall be the most stringent and the device shall be classified in the highest class.
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
Without prejudice to the provisions of article R. 6123-32-9, the provisions of this section do not apply to the health establishments mentioned in the first paragraph of article L. 3211-1 and article…
Authorisation for interventional activity under medical imaging in neuroradiology, category A, may only be granted if the holder draws up an agreement with a structure authorised to carry out interven…
For interventional neuroradiology treatment of cancerous lesions, the holder of the authorisation to carry out interventional neuroradiology activity must hold the authorisation mentioned in 18° of ar…
Interventional procedures under medical imaging in neuroradiology concern diagnostic and therapeutic procedures relating to the cervico-cerebral and medullo-spinal region and which are performed by en…
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