Article R1611-40
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…
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Showing 1671–1680 of 43476 articles for “Art. Art. R 210-4”
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…
The provisions of Articles 1 to 19 and 34 of Regulation (EU) No 2016/425 of the European Parliament and of the Council of 9 March 2016 on personal protective equipment and its annexes constitute the i…
Prior to the conclusion of the contract, the organiser or retailer must communicate the following information to the traveller: 1° The main characteristics of the travel services: a) The destination o…
The three-yearly negotiations on vocational training and apprenticeship cover in particular : 1° The nature of training initiatives and their order of priority; 2° The recognition of qualifications ac…
For the purposes of this Title, the following definitions shall apply 1° Intended use means the use for which a medical device is intended according to the information provided by the manufacturer in…
The Board of Directors of the centres is made up of twenty members, with the exception of centres whose importance or specific nature, particularly with regard to the number of sites or their field of…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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