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Showing 941–950 of 43724 articles for “Art. 815-2”
It is forbidden to mark containers or packaging containing micro-organisms or toxins and products containing them as non-toxic, non-harmful or any other similar indications. Without prejudice to the r…
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 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.
The employer referred to in the third paragraph of article R. 8291-1 shall make a declaration to the union of funds referred to in article R. 8291-2 for each employee seconded to France, prior to the…
External 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 ou…
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…
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