Article D6322-40
When the holder of the authorisation relating to cosmetic surgery facilities is not a public health establishment, the operating area provided for in article D. 6322-33 complies with the provisions of…
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Showing 8941–8950 of 54001 articles for “Art. I-4°”
When the holder of the authorisation relating to cosmetic surgery facilities is not a public health establishment, the operating area provided for in article D. 6322-33 complies with the provisions of…
Each year, before 30 April, the coordination support mechanism sends the regional health agency and, where applicable, the departmental council, an activity report covering, in particular, the achieve…
When the cosmetic surgery facilities are located in a health establishment : 1° The obligations laid down in articles D. 6322-40, D. 6322-41 except for the second paragraph, D. 6322-42 and D. 6322-46…
Health centres set up reception facilities with and without appointment. The days and hours of opening, duty and consultation, the prices charged, the referral system in the event of closure and the m…
The minister responsible for culture may delegate his signature to the prefects for the issue of a cinematographic exhibition permit for cinematographic works of an advertising nature represented in a…
Civil registrars send a birth certificate drawn up in accordance with the provisions of article 11 of decree no. 62-921 of 3 August 1962 amending certain rules relating to civil status records, within…
As part of the pharmacovigilance system, any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 : 1° Implements a risk management system for each medi…
For the medicinal products mentioned in 1° of II of article L. 5121-12 and in II of article L. 5121-12-1, the obligations set out in article R. 5121-161 and articles R. 5121-166 to R. 5121-170 are car…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 shall implement a pharmacovigilance system in order to fulfil its pharmacovigilance obligations…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 is required to: 1° Record all adverse reactions suspected of being due to a medicinal product o…
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