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Showing 1051–1060 of 7976 articles for “Art. BOFiP-RFPI-BASE-20-80”
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…
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.
The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.
When informed of one of the events mentioned in Article L. 5212-2, the Director of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Med…
The information provided for in I and II of Article L. 5232-5 shall be made available in a dematerialised format, accessible free of charge and reusable in such a way as to allow aggregation. To this…
The establishment organises the referral of patients who do not require treatment by the emergency department to another care structure or to a social or medico-social structure, in accordance with pr…
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