Article D4361-20
…ring-aid acoustician has the following equipment: 1° Audioprosthetic measurement equipment : a) A standardised class A tonal and vocal audiometer or an equivalent audiometric unit with outputs for hea…
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Showing 3651–3660 of 64444 articles for “Art. s. 1341-2 and 2224”
…ring-aid acoustician has the following equipment: 1° Audioprosthetic measurement equipment : a) A standardised class A tonal and vocal audiometer or an equivalent audiometric unit with outputs for hea…
…in possession of a guarantee certificate issued by the guarantor, indicating in particular the name and address of the guarantor, the amount, the effective date and the expiry date of the guarantee gr…
The directors of the modelling agency shall include the name and address of their guarantor and the reference to article L. 7123-19 on all documents concerning the agency, in particular on the employm…
The medical file is completed at subsequent visits. At these visits, a new medical fitness form is drawn up and given to the employer and the employee under the same conditions as the initial medical…
The production, manufacture, transport, import, export, possession, offer, transfer, acquisition and use of micro-organisms and toxins or products containing them in a form or under a name liable to c…
…sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines and Health Products).
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…
…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 public health must be subject to a special interve…
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…
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