Article R5222-11
All manufacturers of in vitro diagnostic medical devices, or their representatives, shall appoint a person to be responsible for reactovigilance, whose identity and position shall be communicated to t…
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Showing 9491–9500 of 65809 articles for “Art. R 212-1/2”
All manufacturers of in vitro diagnostic medical devices, or their representatives, shall appoint a person to be responsible for reactovigilance, whose identity and position shall be communicated to t…
Any establishment mentioned in 4° of article R. 5222-3 and any blood transfusion establishment shall appoint a local reactovigilance correspondent.The local reactovigilance correspondent is a doctor o…
The purpose of the certification procedure for the health care organisations and bodies mentioned in articles L. 6113-4 and L. 6147-8 is to assess the quality and safety of the care provided and of al…
Visits are conducted in accordance with professional secrecy. The institution, all the institutions belonging to or associated with the regional hospital grouping or the organisation which is the subj…
The certification procedure established by the Haute Autorité de santé provides in particular for :1° Informing the institution, all the institutions involved or associated with the regional hospital…
The holder of the authorisation for category D ensures, on a permanent basis, in conjunction with the emergency medical assistance service mentioned in article R. 6123-1, the diagnosis and treatment o…
Authorisation for interventional radiology activities may be issued for the following categories : 1° Category A including, with the exception of procedures specifically covered by categories B, C and…
The authorisation holder guarantees that the medical biology tests required for the activity will be carried out within a timeframe compatible with the quality of patient care.
The interventional radiology activity referred to in 21° of article R. 6122-25 includes all medical procedures for diagnostic or therapeutic purposes performed with medical imaging guidance and contro…
The holder of the authorisation for category A has a scanner and an ultrasound scanner on site. The holder of the authorisation for categories B and C has access to : 1° On-site access to a scanner an…
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