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Showing 3791–3800 of 63349 articles for “Art. 3-2° to 4°”
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may prohibit the prescription and supply of a proprietary medicinal product and withdraw it from the mar…
Any change in the marketing authorisation holder is subject to authorisation from the Director General of the Agence nationale de sécurité du médicament et des produits de santé.The application must i…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé shall refuse the marketing authorisation on the grounds mentioned in Article L. 5121-9. The application…
The marketing authorisation holder shall submit to the Director General of the Agence nationale de sécurité du médicament et des produits de santé any proposed amendment to the labelling or package le…
…a of 1° of article L. 6111-2 may be authorised, in application of articles L. 6122-1 and L. 6122-2, to carry out care activities relating to obstetrics, neonatology and neonatal resuscitation.
In order to contribute to improving the safety of pregnancy, birth and the perinatal environment of the mother and child, health establishments practising obstetrics : 1° Participate in the management…
The neonatology unit provides round-the-clock surveillance and the specialised care mentioned in article R. 6123-41 every day of the year, whether or not newborn babies are born in the establishment.…
…newborn babies are born in the establishment's obstetrics unit. This unit is associated with a neonatology intensive care sector on the same site.
The purpose of neonatology is to monitor and provide specialist care for at-risk newborns and those whose condition has deteriorated after birth.
…or this purpose. It can only be carried out if the health establishment includes an authorised neonatology unit on the same site, part of whose facilities are allocated to neonatal intensive care. Eac…
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