Article L5121-7
Non-clinical trials intended to assess the properties and safety of medicinal products for human use must comply with good laboratory practice, the principles of which are laid down by decision of the…
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Showing 4141–4150 of 58479 articles for “Art. Cass. 3e civ. 7-1-1987 n° 85-14.930”
Non-clinical trials intended to assess the properties and safety of medicinal products for human use must comply with good laboratory practice, the principles of which are laid down by decision of the…
The therapeutic indications which may not be advertised to the general public are determined by an order of the Minister for Health issued on a proposal from the Agence nationale de sécurité du médica…
Non-profit humanitarian organisations may have a pharmaceutical establishment, which they own, which wholesales medicinal products to similar organisations with the same purpose in France or in a Stat…
In order to avoid wasting medicines and without infringing on the freedom of medical prescriptions, special arrangements may be laid down by decree for the supply of medicines to beneficiaries of a he…
By way of derogation from the provisions of Article L. 5125-4, for the opening of a pharmacy by way of transfer or grouping within an airport, the number of inhabitants counted is replaced by the annu…
The groups referred to in article L. 5143-6 must be approved by the administrative authority, on the recommendation of committees comprising an equal number of representatives of the administration, r…
The procedures for applying this chapter shall be laid down by decree in the Conseil d'Etat.
When the judicial authority receives a prosecution in application of the articles of this chapter, with the exception of article L. 5423-6, the representative of the State in the département may order…
When a prosecution is brought by the judicial authority in application of the articles in this chapter, the representative of the State in the département may order the temporary closure of the establ…
I.-The criteria for classifying a situation as a risk in the management of a patient's state of health due to the unavailability of an in vitro diagnostic medical device are laid down by regulation.Th…
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