Article R5212-17
Reports are made :1° To the local materiovigilance correspondent when these reports are made by users or third parties who carry out their duties in one of the establishments or associations mentioned…
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Showing 1331–1340 of 3912 articles for “Art. 325-17”
Reports are made :1° To the local materiovigilance correspondent when these reports are made by users or third parties who carry out their duties in one of the establishments or associations mentioned…
The manufacturer or his authorised representative, the importer or the distributor is required to keep, for each incoming and outgoing transaction, at least the following information: 1° The date of t…
For the application of this section, orders issued by the Minister for Health, on a proposal from the Director General of the National Agency for the Safety of Medicines and Health Products, shall spe…
Vigilance includes: 1° For user healthcare professionals mentioned in Article L. 5232-4, the reporting to the Agence française de sécurité sanitaire des produits de santé of any incident consisting of…
The Scientific Advisory Board is responsible for : 1° To ensure the consistency of the Agency's scientific strategy, taking into account recent developments both in methodology and in knowledge of the…
When one or more cases of nosocomial infections have been detected and their nature corresponds to one or more of the reporting criteria defined in article R. 1413-79, the healthcare professional resp…
The terms of cooperation between the SAMU and the SMUR as well as the sectors and terms of intervention of the latter are specified in an agreement or in the network agreement mentioned in article R.…
The National Committee may only deliberate if at least half of the members of the section or configuration convened are present; the quorum is assessed at the beginning of the meeting.However, if the…
In the event of partial or total non-fulfilment of the commitments set out in the contract, the Director General of the Regional Health Agency will send the contract holder a reasoned formal notice to…
Authorisation holders who are not designated under article L. 3221-4 contribute to the implementation of the patient care pathway and carry out their activity in partnership with the establishments pr…
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