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Showing 8301–8310 of 62472 articles for “Art. Décret 55-22 du 4-1-1955”
As part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessm…
For the application of the provisions of this chapter, army hospitals are considered to be public health establishments.
The medical file referred to in article R. 1112-2 must include:identification of the medical device: name, serial or batch number, name of the manufacturer or its authorised representative; - date of…
…g a substance which, if used separately, is likely to be considered as a blood-derived medicinal product. The medical record, if it exists, or, failing this, the document kept by the doctor or dental…
Standby duty is paid at least once a year.
Placing on the market, whether free of charge or for a consideration, a tattoo product whose container or packaging does not bear one of the indications provided for in article R. 513-10-5 is punishab…
Repeated offences under this chapter are punishable in accordance witharticle 132-11 of the French Penal Code.
Decisions to designate candidates are published in the Recueil des actes administratifs of the regional prefecture and on the website of the regional health agency. The decision to designate a candida…
The Director General may declare the call for candidates unsuccessful. In this case, he may designate one or more health establishments providing the public hospital service, in application of 2° of I…
The General Director of the Regional Health Agency's choice of health establishment(s) to be responsible for providing on-call care is based on his assessment, in the light of the applicants' response…
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