Article R7232-20
Any legal entity or sole trader who ceases to fulfil the conditions or respect the obligations mentioned in 4°, 5° and 6° of article R. 7232-17 or who repeatedly fails to respect the obligations defin…
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Showing 921–930 of 3937 articles for “Art. Aut. conc. n° 20-DCC-116”
Any legal entity or sole trader who ceases to fulfil the conditions or respect the obligations mentioned in 4°, 5° and 6° of article R. 7232-17 or who repeatedly fails to respect the obligations defin…
The appeal is lodged, investigated and judged under the conditions laid down by the Code of Civil Procedure for professional elections. The parties are exempted from the requirement to appear before t…
The mediation provided for in Article L. 7345-7 concerning disputes relating to the implementation of a collective agreement in the sector arising between a platform mentioned in Article L. 7343-1 and…
An in-house pharmacy may have legal entities mentioned in article L. 4211-5 provide the following services under the conditions laid down in that article: 1° The supply of gases for medical use to pat…
If the Public Prosecutor considers, following the inspector's report or the laboratory's report, and if necessary after a preliminary investigation, that proceedings should be instituted or an investi…
The medicinal products referred to in this section are kept in a place to which outsiders do not have free access.
On a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the following are set: 1° By order of the Minister for Health: a) The maximum doses…
In application of the fourth paragraph of article L. 5141-5, for the veterinary medicinal products mentioned in this article, the dossier attached to the application for marketing authorisation is com…
All acts relating to the activities mentioned in Article R. 5142-1 or Article R. 5142-40 are carried out under the effective control of a pharmacist or a veterinarian who meets the conditions for prac…
The labelling of a medical device given to the end user or patient, the accompanying leaflet and any other information relating to its operation or use must include a version written in French.
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