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Showing 5741–5750 of 49269 articles for “Art. 635 2-5°”
I.-For the medicinal products of major therapeutic interest referred to in article L. 5111-4, marketing authorisation holders and pharmaceutical companies exploiting medicinal products shall, under th…
Without prejudice to the case where the number of units prescribed corresponds to the number of units appearing in an initial outer packaging that complies with the provisions of article R. 5121-138,…
Any wholesale distributor, where he is not the marketing authorisation holder, who imports a veterinary medicinal product from another Member State shall inform the marketing authorisation holder and…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may grant, under the conditions laid down in Article R. 5211-55 and Article 4 of Implementing Regulation…
The General Director of the Agence nationale de sécurité du médicament et des produits de santé regularly checks that the authorised body has the required skills and up-to-date knowledge of the medica…
The certificate of compliance with good practice relating to raw materials for pharmaceutical use is issued in accordance with Articles R. 5138-3 to R. 5138-6. When the inspection reveals serious brea…
The authorisation holder ensures that each patient's external radiotherapy treatment is carried out by two medical radiation technologists present at the treatment station in the radiotherapy unit.
The holder guarantees the presence of at least one nurse at all times on the site where patients are accommodated.
The coordinating doctor has proven training or experience in addictology.
The authorisation holder offers each patient, depending on their clinical condition, treatment in at least two of the following therapeutic practices: -masso-kinésithérapie; -ergothérapie; -orthophoni…
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