Article R5312-16
The Board of Directors may only validly deliberate if at least ten of its members are present. If this number is not reached, the Board is reconvened within fifteen days. It may then validly deliberat…
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Showing 2571–2580 of 52589 articles for “Art. L 441-10 to L 441-16”
The Board of Directors may only validly deliberate if at least ten of its members are present. If this number is not reached, the Board is reconvened within fifteen days. It may then validly deliberat…
The profession of orthoptist may not be practised in premises or outbuildings of commercial premises. The prohibition set out in the previous paragraph shall not prevent the practice of this professio…
Opticians are identified by wearing a badge showing their surname, first name and professional title.
Voting takes place at the headquarters of the body of the Association concerned or, failing that, at the National Council. The president of the body of the ordre or one of his representatives duly aut…
The dental surgery student gives the employer of the dental assistant being replaced an authorisation issued by the departmental council of the dental surgeons' association of the department in which…
As part of the pharmacovigilance system, any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 : 1° Implements a risk management system for each medi…
The doctor, dental surgeon, midwife, pharmacist or nurse shall immediately report any adverse reaction suspected of being due to a medicinal product or to a product mentioned in article R. 5121-150 of…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 shall implement a pharmacovigilance system in order to fulfil its pharmacovigilance obligations…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 is required to: 1° Record all adverse reactions suspected of being due to a medicinal product o…
I.-Any company or organisation exploiting a medicinal product or a product mentioned in article R. 5121-150 is required to transmit electronically to the European Medicines Agency a periodic safety up…
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