Article R5121-213
The authorisation may be subject to special conditions requiring the beneficiary of the authorisation to implement a plan for monitoring the efficacy and safety of the medicinal product, including the…
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Showing 2011–2020 of 36923 articles for “Art. Cass. com. 21-4-2022 n° 20-16.295”
The authorisation may be subject to special conditions requiring the beneficiary of the authorisation to implement a plan for monitoring the efficacy and safety of the medicinal product, including the…
With the exception of pharmacists covered by the provisions of article L. 4138-2 of the Defence Code, a pharmacist providing a replacement must, in order to do so, apply for registration on the roll o…
The employer is notified of the decision to withdraw the benefit of the exemption. The employer informs the staff representatives. It is also sent to the body responsible for collecting social securit…
No later than two days after recruitment, the employer shall provide the employee with a copy of the second part of the single, simplified declaration enabling the obligations relating to the form, co…
The amount of the financial guarantee may be revised at any time and is reviewed each year. For each modelling agency, this amount may not be less than 6% of the total payroll resulting from the annua…
The medical file is completed at subsequent visits. At these visits, a new medical fitness form is drawn up and given to the employer and the employee under the same conditions as the initial medical…
A prescription for medicinal products in lists I and II may not be made for a treatment period of more than twelve months.However, for public health reasons, in the case of certain medicinal products,…
The production, manufacture, transport, import, export, possession, offer, transfer, acquisition and use of micro-organisms and toxins or products containing them in a form or under a name liable to c…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
The in vitro diagnostic medical devices referred to in Article L. 5221-5 may be exempted from conformity assessment procedures only if the procedure corresponding to the category of device does not in…
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