Article R49-18
Where a deposit has been paid pursuant to the provisions of Article 529-10,the following provisions shall apply: If the deposit is not followed by a request for exoneration or a claim made in accordan…
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Showing 1141–1150 of 48817 articles for “Art. L 227-18 · C. civ. Art. 1843-4”
Where a deposit has been paid pursuant to the provisions of Article 529-10,the following provisions shall apply: If the deposit is not followed by a request for exoneration or a claim made in accordan…
A full pharmacist may only hold direct or indirect shareholdings in four sociétés d'exercice libéral de pharmaciens d'officine other than the one within which he practises. Subject to the ceiling set…
I.-The holder of the "A" authorisation pursuant to Article R. 6123-135 shall have a team comprising: 1° At least one doctor specialising in nuclear medicine present on site during patient care; 2° At…
The holder of the authorisation referred to in Article R. 1131-13 is required to declare to the competent regional health agency and to the Agence de la biomédecine, the names of the approved practiti…
The multidisciplinary clinical-biological medical team referred to in Article L. 2141-2 is composed, for clinical activities involving medically assisted procreation, of at least : 1° A doctor qualifi…
If, at the end of the consultation provided for in article R. 2131-17, it appears to two of the doctors mentioned in 1° of article R. 2131-12 that there is a strong probability that the unborn child i…
I.-A referral to the specialised commercial court pursuant to the third paragraph of Article L. 662-8 is pronounced ex officio by the president of the court seised, by reasoned order, after having hea…
The provisions of articles R. 6523-2-10 to R. 6523-2-14 are applicable, under article L. 6523-1-4, to this sub-section.
I.-The authorisation holder has on site : electro-physiotherapy equipment ; -a balneotherapy facility or a body weight reduction system. II - The authorisation holder provides access, on site or by ag…
The Agence nationale de sécurité du médicament et des produits de santé has a period of four months to evaluate the information provided. At the end of these maximum four months, when, in application…
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