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Showing 1961–1970 of 52521 articles for “Art. 155 IV 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…
…with micro-organisms and toxins or products containing them mentioned in article L. 5139-1 may receive products intended for human or animal consumption.
…toxins which must be subject to the obligation to have a special response plan, depending on the activities carried out, the quantities held or the conditions under which these micro-organisms or toxi…
…gnosis, the manufacturer may also follow one of the three procedures defined in 3° of this article; 2° For in vitro diagnostic medical devices on list A of the order referred to in Article R. 5221-6,…
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…
…biology tests relating to the health plans, actions and programmes mentioned in Article L. 1411-1 ; 2° Medical biology examinations carried out using in vitro diagnostic devices whose performance is e…
…tory with the result obtained by the reference method, where this exists. III -The legal representative of the external quality assessment body shall, at the request of the Director General of the Reg…
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