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Showing 961–970 of 43947 articles for “Art. CE 2-2-1934 n° 30492”
The in vitro diagnostic medical devices referred to in Article L. 5221-5 may be exempted from conformity assessment procedures only if the procedure corresponding to the category of device does not in…
The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.
…eclaration to the union of funds referred to in article R. 8291-2 for each employee seconded to France, prior to the secondment, in order to obtain a professional identification card. Before making th…
…examination is carried out by more than one body, these bodies use a common coding system. The Agence nationale de sécurité du médicament et des produits de santé coordinates the production and updat…
I.-The Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines and Health Products) determines an annual program…
…ally compares the results of each medical biology laboratory with the result obtained by the reference method, where this exists. III -The legal representative of the external quality assessment body…
…ity assessment bodies referred to in article L. 6221-9 must meet the following criteria: 1° Competence, in terms of qualifications and experience, to organise quality control campaigns; 2° Independenc…
The agenda is set by the Chairman. In particular, the agenda must include matters falling within the remit of the committee, the examination of which has been requested by at least half of the full em…
Committee meetings are convened by the Chairman, either on his own initiative or at the written request of at least half of the permanent employee representatives. In the latter case, the committee mu…
…ternal rules shall allocate to each of them a number of seats proportional to its numerical importance, calculated according to the rule of the distribution of the remainders by the highest average. H…
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