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Showing 591–600 of 3386 articles for “Art. 26 mars 2020”
The provisions of this section apply only to medicinal products appearing on the list established by order of the Minister for Health made on a proposal from the Director General of the Agence nationa…
The marketing authorisation is granted by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail. It is accompanied by the summary of pr…
Where the undertaking is operated by a company, the competent corporate body of that undertaking shall appoint, at the same time as the pharmacist or veterinary surgeon in charge and in order to repla…
The manufacturer or his authorised representative shall, for a period of at least five years and, in the case of implantable devices, at least fifteen years after the last copy of the product has been…
In application of Article L. 5212-1, the list of medical devices subject to compulsory maintenance, the list of medical devices subject to internal quality control and the list of medical devices subj…
As part of the EC type-examination procedure, the manufacturer must submit to an authorized body for examination a representative sample, known as the type, of the production envisaged in order that t…
The heavy equipment listed below is subject to the authorisation provided for in Article L. 6122-1:1° (Repealed) ;2° The following cross-sectional imaging equipment, with the exception of that exclusi…
The establishment authorised to carry out the activity mentioned in 3° of article R. 6123-1 sets up or participates in a network with other public and private health establishments. This network contr…
Officers shall at all times treat all persons present at the workplace or in the accommodation of the workers under their supervision with courtesy.
For sedentary staff, weekly rest may be granted on a day other than Sunday for staff whose activities are linked to transport schedules. If they are employed full time, they will benefit from at least…
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