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Showing 2281–2290 of 52609 articles for “Art. 13 §1”
…ucts in article R. 5121-172 ;3° For the homeopathic medicinal products mentioned in article L. 5121-13, after the registration provided for in that article;4° For the traditional herbal medicinal prod…
…ct mentioned in Article R. 5121-150 concerning one or more of these medicinal products or products; 13° "Medication error": an unintentional error by a healthcare professional, a patient or a third pa…
Pharmacovigilance includes: 1° The reporting of adverse reactions suspected to be due to a medicinal product or a product mentioned in article R. 5121-150, including cases of overdose, misuse, abuse a…
This article applies to the post-authorisation safety studies referred to in Article R. 5121-178 which are carried out either voluntarily by the holder of the marketing authorisation referred to in Ar…
The General Manager attends meetings of the Board of Directors in an advisory capacity.
In authorised establishments and in liaison with their directors, the medical managers of transplant activities and those of intensive care and continuous monitoring units draw up agreements defining…
The health care establishment organises a medical service specifically for transplants, provided by a surgeon and a doctor with one of the qualifications mentioned in 3° of article D. 6124-163. It has…
The health establishment authorised to carry out organ transplant activities has the following facilities on site : - the means to ensure extracorporeal blood circulation, long-term mechanical circula…
The number of medical and paramedical staff is adapted to the organ transplant activity and the follow-up of transplant patients. It includes : 1° At least two surgeons who have each completed four ye…
The pharmacovigilance correspondent for blood-derived medicinal products mentioned in article R. 5121-181 is responsible within the establishment for dispensing and monitoring these medicinal products…
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