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Showing 4391–4400 of 31009 articles for “Art. Cass. 3e civ. 31-5-2007 n° 06-12.907”
The preparation, import, export, wholesale distribution and brokering of medicinal products, as well as pharmacovigilance, must be carried out in accordance with good practice, the principles of which…
Two or more pharmacies are authorised to group together if their original location is situated in a municipality with a number of pharmacies in excess of the thresholds provided for in article L. 5125…
Active substances may only be imported from third countries if they have been manufactured in accordance with standards of good practice at least equivalent to those laid down by the European Union, a…
I. - In addition to their obligations under Article 23 of the above-mentioned Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009, any responsible person and…
The inspectors referred to in article L. 5127-1 may not engage in any other professional activity, unless it is carried out exclusively in a health establishment. However, they may belong to the teach…
I.-The retail supply, whether free of charge or for consideration, of:1° Medicated feedingstuffs as provided for in Article 16 of Regulation (EU) 2019/4 of 11 December 2018;2° Veterinary medicinal pro…
The Agence nationale de sécurité du médicament et des produits de santé and the administrative authority referred to in II of Article L. 5211-2, within their respective areas of competence, may, under…
If the availability of veterinary medicinal products is insufficient to meet the requirements of the fight against an epizootic disease, the Minister for Agriculture may, with a view to ensuring that…
The terms and conditions for the application of this chapter shall, where necessary, be determined by decree in the Conseil d'Etat.
In the interests of public health, decrees issued by the Minister for Health shall, where necessary, lay down specific conditions relating to the supply of the devices referred to in article L. 5211-1…
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