Article R5121-147
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
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Showing 2961–2970 of 64840 articles for “Art. L 581-7 and L 581-14”
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
For medicinal products containing radionuclides, in addition to the information provided for in article R. 5121-140, the labelling of the protective shielding provides all the explanations relating to…
When the application is submitted, the applicant assigns an internal reference number to each of the advertising media, in accordance with the rules defined by a decision of the Director General of th…
The provisions of articles R. 5125-15 to R. 5125-24 govern companies formed pursuant to Title I of law no. 90-1258 of 31st December 1990 relating to the practice in the form of companies of liberal pr…
The deliberations of the joint committee set up by article 2 of the agreement of 31 December 1958 and relating to the scope of application of the approved agreement are subject to the approval of the…
During the term of the agreement, the apprentice continues to follow the courses provided by the training centre in which he is registered. They must comply with the host company's internal rules.
Employees under the age of twenty-six who are holders of a professionalisation contract receive a minimum wage for the duration of the fixed-term employment contract or the professionalisation action…
The training plan is sent, together with the trainee's application for remuneration, under the conditions set out in 1° of article R. 6341-33.
The Directorate General for Labour :1° Determines labour policy guidelines, coordinates and evaluates actions, particularly with regard to monitoring the application of labour law;2° Contributes to de…
A copy of the report or record of sampling shall be sent by its author(s), as appropriate, to the Director General of the Agence nationale de sécurité du médicament et des produits de santé or to the…
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