Article R7122-25
The State-authorised body referred to in article L. 7122-23 sends the regional prefect the information required to verify compliance with the annual ceiling referred to in article R. 7122-13.
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Showing 4251–4260 of 36791 articles for “Art. Cass. com. 24 November 1992 n° 91-11.055 · CA Dijon 12 October 1995 · CA Paris 25 October 2000 · Cass. com. 22 November 2016 n° 14-23.658 · CA Versailles 19 January 2016 · Cass. com. 8 July 1997 · Cass. com. 14 November 2019 n° 18-16.807”
The State-authorised body referred to in article L. 7122-23 sends the regional prefect the information required to verify compliance with the annual ceiling referred to in article R. 7122-13.
…heir activities in the field of child protection or by their interest in the minors concerned. Applicants may be heard by the committee if they so wish. They may be assisted or represented by a person…
…relations sociales des plateformes d'emploi, which is responsible for examining the declaration of candidacy, will issue an electronic receipt to the representative of the candidate organisation as s…
…ts, including those prepared on an ad hoc basis as referred to in 4° and 5° of the I of Article R. 5126-9, the in-house pharmacy may organise, on the basis of an agreement, with an establishment or bo…
If the experts disagree, they appoint a third party expert. If no agreement can be reached on the choice of this third party expert, he will be appointed by the president of the court. The third party…
The coloured net provided for in article R. 5132-15 is red for List I medicinal products and green for List II medicinal products.
Establishments in which operations are carried out on micro-organisms or toxins included on the list drawn up in application of article L. 5139-1 and identified as presenting the highest risks to publ…
Where the conformity certification procedure applied by a manufacturer involves the intervention of an authorized body, the manufacturer may apply to the body of his choice within the framework of the…
The operator must ensure that the maintenance and quality controls required for the medical devices it operates are carried out. Maintenance is carried out either by the manufacturer or under his resp…
Only health establishments authorised to carry out the activity mentioned in 3° of article R. 6123-1 inform the public that they provide emergency services and display an "emergency" sign. In the case…
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