Article D1221-15
Blood and its components may only be used to prepare in vitro diagnostic medical devices if the results of the tests and analyses provided for in b, c and d of 5° of Article D. 1221-6 are negative. Ho…
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Showing 1171–1180 of 20457 articles for “Art. n° 15-21.478 + Cass. 3e civ.”
Blood and its components may only be used to prepare in vitro diagnostic medical devices if the results of the tests and analyses provided for in b, c and d of 5° of Article D. 1221-6 are negative. Ho…
The establishment's funds may be deposited in a banking institution, with the authorisation of the Minister responsible for the budget.
Any establishment or organisation planning to carry out research requiring the use of an organ removed from a person whose death has been duly confirmed must send the Director General of the Agence de…
I.-The applicant establishments or organisations have medical, paramedical and technical staff who carry out their duties under the authority of the person in charge or the person responsible for the…
I. - The application for authorisation provided for in the second paragraph of I of Article L. 1245-5 for products from Member States of the European Union or parties to the Agreement on the European…
The health inspection referred to in 2° of I of article L. 1321-4 is carried out by the Regional Health Agency. It includes any operation to check compliance with legislative and regulatory provisions…
The Board of Directors may delegate certain of its powers to its Chairman or to the Chief Executive Officer, with the exception of the matters referred to in 1°, 3°, 4°, 6°, 7°, 10°, 18° and 20°, with…
The health and hygiene rules laid down by this section apply to residential premises, as well as to the surroundings of these premises and to the common areas of multi-family residential buildings. Th…
Before issuing the authorisation provided for in Article R. 1333-148, the person responsible for the nuclear activity :1° Verify that the person concerned needs, in the course of his or her activity,…
All imports or exports of radioactive sources from or to non-EU countries must be registered in advance with the Institut de Radioprotection et de Sûreté Nucléaire.The exporter or importer completes a…
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