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Showing 4711–4720 of 11432 articles for “Art. CE 17-10-1990 n° 56991”
…Health Products.The decision of the Director General of the Agency is taken within ninety days of receipt of the complete application. If no decision has been taken by the end of this period, the appl…
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…
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…
…diology activities may be issued for the following categories : 1° Category A including, with the exception of procedures specifically covered by categories B, C and D, endovenous interventional radio…
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.
…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 control b…
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…
In the performance of their duties, authorised agents may record infringements and breaches of Chapters I and III of Title I, and Chapters I, II, III, and IV of Title II of the loi n° 78-17 du 6 janvi…
The enforcement measures provided for in Article L. 412-1 : 1° The provisions of Articles 1 and 7 of Commission Regulation (EEC) No 2568/91 of 11 July 1991, as amended, on the characteristics of olive…
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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