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Showing 4491–4500 of 67437 articles for “Art. I-5° bis and Art. 35 bis”
The Agence nationale de sécurité du médicament et des produits de santé and the administrative authority referred to in II of Article L. 5211-2, within their respective areas of competence, may, under…
…entilation system must certify that it complies with the requirements mentioned in 1° of article R. 3512-4. The person in charge of the establishment is required to produce this certificate for any in…
…scular rehabilitation, subject to the provisions of article R. 4321-8 ; f) Re-education of vascular and lymphatic trophic disorders; 2° Re-education concerning after-effects : a) Re-education of amput…
…41-2 or providing services associated with these veterinary medicinal products, financial penalties and, where appropriate, daily fines in the event of failure to comply with the following obligations…
…e union of funds mentioned in article R. 8291-2 draws up a report on the application of this system and sends it to the Minister for Employment.
…for in article L. 1525-5 have been committed: a) Either using false or inaccurate weights, measures and other instruments; b) Or using manoeuvres or procedures designed to distort the operations of an…
The manufacturer undertakes to fulfil all the conditions necessary for the approved quality system to remain effective.
…lication for assessment of the quality system listed in article R. 4313-44 as well as the decisions and reports provided for in articles R. 4313-48, R. 4313-49, R. 4313-53 and R. 4313-54.
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
…er must allow the notified body access to the locations of design, manufacture, inspection, testing and storage and must provide all necessary information, in particular: 1° the documentation on the q…
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