Article R1413-44
In order to carry out the tasks and powers provided for in Articles L. 1413-1, L. 1413-2 and L. 1413-3, the Director General of the Agency shall enter into an agreement with each Director General of a…
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Showing 1641–1650 of 42843 articles for “Art. R 134-4”
In order to carry out the tasks and powers provided for in Articles L. 1413-1, L. 1413-2 and L. 1413-3, the Director General of the Agency shall enter into an agreement with each Director General of a…
I.-For the application of 3° of a of article L. 3332-1, the department may allocate to reserves a fraction of the revenue from transfer duties for valuable consideration that it recognises in respect…
I.-When a private health care institution is authorised to provide the public hospital service under the conditions defined in article L. 6112-3, its legal representative must bring its articles of as…
I. - Each Specialised Commission shall meet when convened by the Chairman of the Autorité des marchés financiers or at the request of half of its members. In the event of absence, the Chairman of the…
For the application of the second paragraph of article L. 2333-38 in respect of the tourist tax and of article L. 2333-46 in the case of flat-rate tourist tax, the notice of compulsory taxation must i…
Manufacturers of veterinary medicinal products mentioned in 1° of article R. 5142-1 must justify, at all times, that all the products they use, manufacture and deliver comply with the characteristics…
When it is consulted pursuant to IV of article L. 1611-10, the Consultative Commission on the Financial Responsibility of Local Authorities shall give its opinion within three months of the date of re…
For the purposes of this Title, the following definitions shall apply 1° Accessory means any article which is intended by its manufacturer to be used principally with an in vitro diagnostic medical de…
The members of the Supervisory Board of public health institutions, including those with national or inter-regional jurisdiction, are appointed by order of the Director General of the Regional Health…
As part of the EC declaration of conformity procedure, production quality assurance, for active implantable medical devices or medical devices in class IIb or class III, the manufacturer submits an ap…
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