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Showing 8291–8300 of 62472 articles for “Art. Décret 55-22 du 4-1-1955”
…tatute for Civil Servants and the legal and regulatory provisions applying to public employees. The duties, tasks and obligations of the directors of the institutes or schools referred to in the first…
…wable on application by the holder to the National Agency for the Safety of Medicines and Health Products no later than nine months before its expiry date. The application for renewal is accompanied b…
The committee responsible for proposing the list of approved products for public authorities, in accordance with the provisions of articles L. 5123-2 and L. 5123-3, is the Transparency Committee, the…
When, for a period exceeding one month, an assistant pharmacist, recruited in application of articles R. 5124-38 or R. 5124-39, is absent or replaces the responsible or delegated pharmacist, he is rep…
…rganisations mentioned in article R. 5124-2 take the necessary measures to ensure that medicinal products and other pharmaceutical products are transported and delivered under conditions that guarante…
For the purposes of the third paragraph of Article L. 5125-25, a sealed package is any opaque package bearing the name of a single patient and sealed in such a way that the recipient can ensure that i…
…article R. 5127-13, a sample consists of three samples, one left with the owner or holder of the product, the second destined for the laboratory competent to carry out the analyses and the third retai…
As part of the EC declaration of conformity procedure, production quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the…
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
As part of the EC verification procedure, the manufacturer submits the devices manufactured for inspection by an authorised body. The authorised body checks the conformity of the medical devices with…
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