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Showing 1621–1630 of 38032 articles for “Art. L 227-14”
The sponsor shall provide the investigators of chemical, pharmaceutical, biological, pharmacological or toxicological tests with:1° The title and objective of the test requested ;2° Identification of…
At least fifteen days before the date of the elections, the President of the body of the Order concerned or, failing this, the President of the National Council, will send all voters a list of candida…
The regional directorate for youth, sport and social cohesion provides the committee's secretariat.
The presence of an information leaflet for the user in the packaging of any medicinal product or product is compulsory, unless the information referred to in article R. 5121-149 appears directly on th…
The information provided for in Articles R. 5121-138 and R. 5121-139 is written in French. They may also be written in other languages, provided that the same information appears in all the languages…
Ampoules or other small primary packaging on which it is impossible to include all the information specified in Article R. 5121-138 may bear only the following information: 1° The name of the medicina…
By way of derogation from the provisions of Article R. 5121-138, when the medicinal products or products are contained in an outer packaging that complies with the requirements of the said Article, th…
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
For medicinal products containing radionuclides, in addition to the information provided for in article R. 5121-140, the labelling of the protective shielding provides all the explanations relating to…
The package leaflet is drawn up in accordance with the summary of product characteristics. It includes a standard text, expressly inviting patients to report any suspected adverse reaction to their do…
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