Article R5141-123-18
The holder of a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse…
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Showing 1171–1180 of 7327 articles for “Art. 18 March 2020”
The holder of a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse…
…lect revenue and authorise expenditure under the conditions mentioned in 1° to 4° of article R. 712-18 taking as a reference the aggregate of the initial budgets or latest amending budgets approved by…
When the valuation is carried out in accordance with 2° of Article L. 214-24-15, the AMF may require that the valuation procedures implemented by the AIF or its management company, as well as the valu…
…place of death or in the nearest space set aside for this purpose referred to in l'article L. 2223-18-2.
An employer is deemed to be in a state of insolvency within the meaning of Article L. 3253-18-1 when an application has been made to open collective proceedings based on the employer's insolvency, as…
…ode, who can prove that they have completed a traineeship meeting the conditions of articles R. 812-18-3 and R. 812-18-4, which may not be less than thirty months, in the office of a judicial represen…
…ies are practised, as well as its annexes, without the authorisation provided for in article L. 232-18-7. They may obtain explanations on site between 6am and 11pm, or at any time when these premises…
…2-9, with the exception of narcotics, where applicable by applying the provisions of article L. 232-18-5. These acts may not constitute incitement to commit an offence, failing which they shall be nul…
…the trainee of all the legal and management acts mentioned in the first paragraph of article R. 812-18-2; it also includes the assessments of the quality of his work by the training supervisor and the…
The provisions of this section do not apply when : 1° The device is sold to a manufacturer of an in vitro diagnostic medical device, except where the latter expressly requests this from the reseller;…
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