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Showing 1731–1740 of 38045 articles for “Art. L. 441-14”
…for opinions for the most frequent operations meeting the characteristics specified in this protocol. In this case, for all the dossiers and operations meeting these characteristics, the company send…
The CE marking may be affixed to a medical device only if it complies with the essential health and safety requirements referred to in Section 5 of this Chapter and has undergone the certification pro…
Manufacturers or their agents, importers and distributors shall declare without delay to the Director General of the Agence nationale de sécurité du médicament et des produits de santé any incidents o…
The provisions of articles R. 5211-15, R. 5211-17, R. 5211-19 and R. 5211-20 are applicable to in vitro diagnostic medical devices.
In order to provide the most appropriate equipment for the needs of the person who is ill or has an incapacity or disability, the service provider and the equipment distributor will ask the prescriber…
In health care institutions, the collection of information concerning nosocomial infections which must be reported in accordance with article R. 1413-79 is organised according to procedures defined by…
The location of the SMURs mentioned in 2° of article R. 6123-1 is determined by the regional health plan and ensures territorial coverage.
Attached to the contract are the health project, a list of agreements and other valid contracts signed by the holder with the regional health agency, and any financial agreements signed with bodies ot…
The purpose of the "ante- and post-partum" hospital at home activity is to provide hospital at home care for women before and after childbirth.
The activity of medicine consists of the general or specialised care, for diagnostic, therapeutic or palliative purposes, of patients whose state of health requires care or monitoring of a medical nat…
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