Article R2311-15
Any centre which decides to carry out the screening or treatment activities referred to in Article R. 2311-14 is required to make a declaration to the Director General of the Regional Health Agency, w…
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Showing 4601–4610 of 59903 articles for “Art. R 227-1-1”
Any centre which decides to carry out the screening or treatment activities referred to in Article R. 2311-14 is required to make a declaration to the Director General of the Regional Health Agency, w…
The contract is signed no later than one month after the diagnosis is carried out, on behalf of the State, by the legal representative of the local mission or any employee duly authorised by him/her a…
The vigilance exercised over cosmetic products by the Agence nationale de sécurité du médicament et des produits de santé includes : 1° Receiving and recording serious adverse reaction reports sent by…
The establishment authorised to provide systemic medicinal treatments for cancer with a C rating complies with the obligations imposed on holders of authorisations for medicine caring for children and…
In article R. 713-1-1:a) In the first, third and fourth paragraphs, the words: "chambre de commerce et d'industrie territoriale" are replaced by the words: "chambre d'agriculture, de commerce, d'indus…
I.-An order of the Minister for Defence and the Minister for Health determines the compulsory terms of the agreement provided for in I of article L. 6147-10 and in particular, under the conditions pro…
I.-For the contracts referred to in article R. 113-11, where the conditions for cancellation provided for in article L. 113-15-2 are met, the insurer shall apply the provisions of that article:1° When…
I.-The Chairman of the Board of Directors is appointed for three years, in accordance with the conditions set out in article L. 6123-7.II - The Chairman of the Board of Directors :1° Chairs the discus…
The National Designs Register is kept by the National Institute of Industrial Property. It contains, for each filing: 1° The identification of the holder and the references of the filing as well as su…
An accelerated assessment procedure may be set up under conditions defined by order of the Minister for Health when the clinical trial of medicinal products takes place in the context of an emergency…
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