Article R4451-105
The employer shall inform the labour inspector referred to in Article L. 8112-1 and, as appropriate, the Nuclear Safety Authority or the delegate for nuclear safety and radiation protection for defenc…
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Showing 921–930 of 64807 articles for “Art. Cass. 3e civ. 1-2-2012 n° 10-22.863”
The employer shall inform the labour inspector referred to in Article L. 8112-1 and, as appropriate, the Nuclear Safety Authority or the delegate for nuclear safety and radiation protection for defenc…
The heads of external companies must inform the user company in writing of: 1° The date of their arrival and the foreseeable duration of their work; 2° The foreseeable number of workers assigned; 3° T…
Any employer who intends to carry out work in the vicinity of electrical lines or installations shall obtain information from the operator, whether the local representative of the energy distribution…
To determine the minimum distances to be observed in relation to normally energised bare conductive parts, account must be taken of: 1° All possible movements of the energised bare conductive parts of…
The professional practice standard relating to the probative nature of evidence gathered (specific applications), approved by the Minister of Justice, is shown below:PROFESSIONAL PRACTICE STANDARD REL…
The safety study includes all the information required to enable the head of the company carrying out the work to define and implement the necessary preventive measures to ensure the safety and protec…
The temporary cessation of activity following the formal notice procedure provided for in articles R. 4721-6 et seq. is the subject of a reasoned decision including the factual and legal elements char…
Nurses always act in the patient's best interests. Their care is conscientious, attentive and based on scientific knowledge. They devote the necessary time to this task, using the most appropriate sci…
A medicinal product or a series of medicinal products mentioned in Article L. 5121-13 may only be registered if the applicant is established in a Member State of the European Community or a party to t…
The application file for registration of a medicinal product or a series of medicinal products mentioned in article L. 5121-13 is sent to the Agency. It includes the following information and document…
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