Article R5212-15
The following incidents may be reported: 1° A noxious and unintended reaction occurring during the use of a medical device in accordance with its intended purpose; 2° A noxious and unintended reaction…
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Showing 3121–3130 of 68984 articles for “Art. 494-1 al. 1 and al. 2”
The following incidents may be reported: 1° A noxious and unintended reaction occurring during the use of a medical device in accordance with its intended purpose; 2° A noxious and unintended reaction…
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 reports, whether mandatory or optional, provided for in articles R. 5212-14 and R. 5212-15 are made by manufacturers or their representatives, users or third parties who observe or are aware of in…
When the facts mentioned in Article L. 5212-2 are brought to the attention of the Director General of the Agence nationale de sécurité du médicament et des produits de santé by a user or a third party…
Incidents or risks of incidents as defined in Article L. 5212-2 must be reported immediately.
I.-The agreement establishing the regional hospital grouping consists of two parts: 1° The section relating to the shared medical project provided for in I of Article L. 6132-1 ; 2° The section relati…
…the letter rogatory, the judicial police officer may have the operations provided for in Article 55-1.The provisions of the last four paragraphs of Article 55-1 shall apply. The authorisation provided…
…by a reasoned decision, oppose the registration of an athlete on the lists mentioned in article L. 221-2 when one of the conditions mentioned in 1° and 2° of article R. 221-15 is met.
After cremation, the ashes are pulverised and collected in a cinerary urn with a plaque on the outside bearing the identity of the deceased and the name of the crematorium.Pending a decision on the de…
…veterinary medicinal product which has already been the subject of a parallel import authorisation, and the proprietary veterinary medicinal product which is the subject of the application comes from…
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