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 711–720 of 22933 articles for “Art. Cass. com. – 25 Sept. 2012 – no. 11-22754”
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.
The directors of the modelling agency shall include the name and address of their guarantor and the reference to article L. 7123-19 on all documents concerning the agency, in particular on the employm…
Reasons must be given for refusing or withdrawing individual authorisations and approvals. Reasons may be given at the request of persons qualified by their activities in the field of child protection…
The Autorité des 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 o…
For advanced therapy medicinal products, 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 a…
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…
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