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Showing 7881–7890 of 69207 articles for “Art. s. L 313-10 and R 313-8 to R 313-10”
The declarations and the periodic safety update report referred to in Articles R. 5121-161, R. 5121-168 and R. 5121-170 are drawn up in accordance with the procedures and standard form laid down by th…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 implements procedures to obtain accurate and verifiable information for the scientific evaluati…
The in-house pharmacies referred to in Article L. 5126-1 shall forward to the Director General of the Agence nationale de sécurité du médicament et des produits de santé, immediately upon request, a r…
The procedures and standard form for the declarations and report mentioned in Articles R. 5121-174 to R. 5121-176 are laid down by decision of the Director General of the Agence nationale de sécurité…
The use of radioscopy equipment without an automatic dose rate control device or without an image intensifier or equivalent device is prohibited.
Any medical device exposing patients to ionising radiation complies with the regulatory provisions adopted in application of Article L. 5212-1.Medicinal products and radiopharmaceuticals are used in a…
The dismissal of the employee representative appointed pursuant to article L. 621-4 is governed by the provisions of articles R. 436-1 to R. 436-8 and article R. 436-10 of the Labour Code.
The decisions of the Autorité de la concurrence referred to in Article L. 470-7-1 are published on the Autorité's website. Publicity may be limited to take account of the legitimate interest of the pa…
The provisions of articles R. 2172-8 to R. 2172-10 apply.
When the French Anti-Doping Agency decides to reject or grant an application for recognition of a Therapeutic Use Exemption issued by an International Federation or a body referred to in 4° of article…
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