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Showing 4621–4630 of 53829 articles for “Art. R. 210-2”
…vitro diagnostic medical device with the essential requirements set out in Section 5 of this Chapter. He shall specify the principles for ensuring the quality of his production and guarantee that his…
I.-External quality control of medical devices is carried out by bodies accredited for this purpose by the Comité français d'accréditation or by any other accreditation body which is a signatory to a…
…ese examinations and tests are carried out is agreed between the authorized body and the manufacturer. Where the type meets the essential requirements, the authorised body issues the applicant with an…
The Agency's inspectors shall carry out inspections as decided by the Agency's Director General, who shall issue a letter of assignment to the inspector in charge of the investigation. This letter spe…
On the basis of a contract that complies with good hospital pharmacy practice, the principles of which are laid down by order of the Minister for Health, and after obtaining the opinion of the regiona…
The safety of healthcare establishments in the event of a failure in the energy network is ensured under the conditions set out in sub-section 1 of section 4 of chapter II of title III of book VII of…
The authorisation holder shall carry out the assessment referred to in Article L. 6122-5, in accordance with the conditions laid down in this section.The purpose of this evaluation is to check that th…
The national committee draws up its own rules of procedure, which are submitted to the ministers responsible for social action, health and social security for approval.
The health care organisation organises the coordination of patient care between the emergency department and the other acute care or follow-up departments in the health care organisation if it has one…
Applications for authorisation and, where appropriate, for renewal of authorisation are sent to the Director General of the Regional Health Agency by electronic means or by registered post with acknow…
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