Article R4221-7-1
For each session, an order by the Minister for Health decides on the organisation of tests in pharmacy and medical biology and determines the number of places available and the list of host structures…
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Showing 7491–7500 of 52212 articles for “Art. 1844-1”
For each session, an order by the Minister for Health decides on the organisation of tests in pharmacy and medical biology and determines the number of places available and the list of host structures…
In order to avoid any deterioration in the health of workers as a result of their work, the occupational physician or, in inter-company occupational health and prevention services, the multidisciplina…
The prescription for a route is valid for up to twenty-four months from the date of issue of the receipt referred to in the last paragraph of article R. 5132-1-6.
A person who has benefited from a pathway to integration through economic activity is not eligible for a new pathway within two years of the end of their previous pathway or, if the pathway has been t…
The prescription of a pathway is suspended when the work contract within a structure mentioned in article L. 5132-4 is suspended for more than 15 days, broken or terminated. The suspension is declared…
I. - The chiropodist is free to communicate to the public, by any means, including on a website, information likely to contribute to the patient's free choice of practitioner, relating in particular t…
I.-When France Compétences revises the recommendations during the two-year period provided for in IV of article D. 6332-78-1 and V of article D. 6332-79, it invites the professional branches, by any m…
I. - France Compétences invites the branches, by any means that provides a definite date of receipt of this request, to determine the level of funding for apprenticeship contracts, in accordance with…
I. - Before issuing the authorisation applied for, the Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines a…
The clinical evaluation and its results are included or duly referenced in the technical documentation for the device referred to in Article R. 5211-39. The clinical evaluation and its documentation a…
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