Article R7232-22
In the case provided for in the first paragraph of Article L. 7232-8, the legal entity or sole trader who has been the subject of a decision to withdraw the benefit of Articles L. 7233-2 of the Labour…
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Showing 901–910 of 3456 articles for “Art. n° 22-14.091”
In the case provided for in the first paragraph of Article L. 7232-8, the legal entity or sole trader who has been the subject of a decision to withdraw the benefit of Articles L. 7233-2 of the Labour…
I.-The platform or the representative appointed pursuant to Article L. 7343-12 who withdraws from the mediation shall inform the Autorité des relations sociales des plateformes d'emploi, which shall t…
The categories of preparations referred to in 2° of Article L. 5126-5 which an internal-use pharmacy of a health care establishment may entrust by written contract to a pharmaceutical establishment au…
Pharmacists are only authorised to dispense these medicines for the first time on presentation of a prescription less than three months old. List I medicinal products may only be renewed if the prescr…
When an expert opinion has been requested, two experts are appointed, one by the examining magistrate and the other by the person concerned. The investigating magistrate will set a time limit for the…
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…
When informed by the holder of a marketing authorisation granted under 1°, 2° or 3° of Article R. 5141-20, before the marketing of the veterinary medicinal product concerned, of the fact that for all…
A pharmacist or veterinary surgeon in charge or delegate registers with the order to which he belongs, and registers his diploma, under the conditions provided for in article L. 4221-16 for pharmacist…
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
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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