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Showing 6351–6360 of 52239 articles for “Art. 35 I 5° bis”
An individual assessment of the beneficiary's social and professional situation and needs is carried out by a prescriber or a structure for integration through economic activity before the person is d…
Where batches of investigational medicinal products come from another Member State of the European Community or party to the Agreement on the European Economic Area and are manufactured or imported in…
Before removing or partially or totally covering the safety features provided for in article R. 5121-138-2, the pharmaceutical establishment which manufactures medicinal products shall check that the…
By way of derogation from the provisions of the first sub-section, the provisions of this sub-section apply to the manufacture and importation of investigational medicinal products.
For investigational medicinal products, the documents relating to each batch are kept by the pharmaceutical establishment which manufactures it, for at least five years after the end of the trial or t…
The manufacturer or importer of investigational medicinal products shall ensure that all manufacturing operations are carried out in accordance with the information provided by the sponsor in the appl…
The holder guarantees the presence of at least one nurse at all times on the site where patients are accommodated.
Hospital practitioners who, as contract practitioners or hospital assistants, have signed a hospital career commitment agreement in application of the provisions of article R. 6152-404-1 or article R.…
I.-The duties of director, member of the Supervisory Board and mutual agent are free of charge.However, if the Articles of Association so provide, the Board of Directors or the Supervisory Board may d…
Prior to their appointment, all external valuation experts shall inform the open-ended real estate investment company or the fund management company whether or not they have taken out an insurance pol…
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