Article R5121-217
For the application of the provisions of this chapter, army hospitals and the army blood transfusion centre shall be regarded as health establishments and a blood transfusion establishment respectivel…
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Showing 3171–3180 of 47145 articles for “Art. Cass. ass. plén. 21 December 2007 n° 06-11.343 · Cass. 3e civ. 24 April 2003 · Cass. 3e civ. 4 October 1995 · Cass. 3e civ. 7 June 2000 · Cass. 3e civ. 29 November 2000 · Cass. 1re civ. 6 November 2002”
For the application of the provisions of this chapter, army hospitals and the army blood transfusion centre shall be regarded as health establishments and a blood transfusion establishment respectivel…
The Agence de la biomédecine is informed of the decisions taken in application of Article R. 5121-212.
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…
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…
…to the form, content and transmission of the fixed-term employment contract set out in Articles L. 1242-12 and L. 1242-13 to be met.
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…
The time limits set by articles R. 7343-16 and R. 7343-18 to R. 7343-20 are calculated and extended in accordance with the provisions of articles 640 to 642 of the Code of Civil Procedure.
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…
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