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Showing 1791–1800 of 29147 articles for “Art. s. 1832 to 1844-17”
In the event of failure to comply with the legislative and regulatory requirements, the conditions for granting or monitoring the authorisation referred to in Articles R. 5121-212 and R. 5121-213, or…
…ust be accompanied by a technical dossier, the model for which is laid down by decision of the Director General of the National Agency for the Safety of Medicines and Health Products.The decision of t…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision within a maximum of one hundred and twenty days from the date…
Distributions of profits made by companies that have entered into an agreement with the Minister of the Economy and Finance in accordance with the provisions of l'ordonnance n° 59-248 du 4 février 195…
The provisions of sub-section 2 of section 7 of this chapter relating to cancer treatment activities are applicable to the holder of the authorisation under grades C and D when it carries out interven…
…ges of intra-thoracic, intra-abdominal or intra-pelvic organs; 2° Category B including, in addition to the procedures authorised under category A, and with the exception of procedures specifically cov…
The authorisation holder guarantees that the medical biology tests required for the activity will be carried out within a timeframe compatible with the quality of patient care.
The interventional radiology activity referred to in 21° of article R. 6122-25 includes all medical procedures for diagnostic or therapeutic purposes performed with medical imaging guidance and contro…
I. - The holder of the authorisation for category A has access to a continuous monitoring unit on site or by agreement, under conditions that allow the patient to be cared for within a timeframe that…
The provisions of Article R. 6123-161 and those of 2° of Article R. 6123-162 do not apply to the heavy equipment mentioned in Article L. 6122-14-1.
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