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Showing 861–870 of 20118 articles for “Art. Cass. com. 20 mars 2007 n° 05-19225”
Each chemical, pharmaceutical, biological and non-clinical trial gives rise to a report drawn up by the investigator who carried out the trial. This report, dated and signed, states in particular: 1°…
To be eligible for election as a member of the Disciplinary Board, a pharmacist must on the closing date for the submission of candidacies:1° Be a voter under the Order of Pharmacists of New Caledonia…
…reasoned decision, refuse to include a medicinal product on the list referred to in Article R. 5121-202 for any public health reason, in particular when the benefit/risk balance of the medicinal produ…
The detailed rules for the application of sections 1 to 12 of this chapter are determined as necessary, after obtaining the opinion of the Director General of the Agence nationale de sécurité du médic…
Blood establishments and organisations or companies manufacturing or exploiting blood-derived medicinal products which are aware of information likely to cast doubt on the quality of blood or plasma i…
…on of these articles, the authorisation for these preparations is that mentioned in article R. 5121-207.
The Director General of the Agence nationale de sécurité du médicament et des produits de santé shall draw up the list of medicinal products, known as medicinal products for officinal use, which the d…
The application for authorisation or renewal of authorisation provided for in 12° and 13° of Article L. 5121-1 shall be sent by registered post with acknowledgement of receipt or lodged against receip…
For the purposes of this sub-section, army hospitals and the army blood transfusion centre are regarded as public health establishments and blood transfusion establishments respectively.
The application to obtain the endorsement referred to in Article R. 5122-19 shall be sent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé by the manu…
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