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Showing 4491–4500 of 46101 articles for “Art. CA Paris 13-2-2023 n° 21/01048”
…organisms or toxins and products containing them as non-toxic, non-harmful or any other similar indications. Without prejudice to the regulations concerning the transport of dangerous goods, container…
No container or packaging that has been in contact with micro-organisms and toxins or products containing them mentioned in article L. 5139-1 may receive products intended for human or animal consumpt…
Establishments in which operations are carried out on micro-organisms or toxins included on the list drawn up in application of article L. 5139-1 and identified as presenting the highest risks to publ…
For the purposes of placing on the market in vitro diagnostic medical devices other than those subject to a performance evaluation, manufacturers shall follow the following procedures: 1° For in vitro…
The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.
…ach employee seconded to France, prior to the secondment, in order to obtain a professional identification card. Before making the declaration provided for in the previous paragraph, the employer shal…
…xternal quality assessment bodies use a coding system to identify the techniques used in the analytical phase of each examination. Where quality control of a medical biology examination is carried out…
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…
I.-Medical biology laboratories shall submit each analytical system they use to an external quality assessment. II.-Each external quality assessment body for medical biology examinations mentioned in…
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…
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