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Showing 1301–1310 of 4038 articles for “Art. 17 Dec 1990”
…rt, is accompanied by a curriculum vitae. Where applicable, professional links with the sponsor are declared.
The period of practical experience provided for in article R. 5142-16 is reduced : 1° To one year for professionals whose higher education was completed as part of a five-year programme ; 2° To six mo…
No medical device may be placed on the market or put into service in France unless it complies with the essential health and safety requirements referred to in section 5 of this chapter which apply to…
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 manufacturer or his authorised representative, the importer or the distributor is required to keep, for each incoming and outgoing transaction, at least the following information: 1° The date of t…
For the application of this section, orders issued by the Minister for Health, on a proposal from the Director General of the National Agency for the Safety of Medicines and Health Products, shall spe…
…ty of use of the health products mentioned in this section; c) The monitoring of corrective actions decided upon; 3° For manufacturers, publishers, distributors and users, the communication of the inf…
The Scientific Advisory Board is responsible for : 1° To ensure the consistency of the Agency's scientific strategy, taking into account recent developments both in methodology and in knowledge of the…
When one or more cases of nosocomial infections have been detected and their nature corresponds to one or more of the reporting criteria defined in article R. 1413-79, the healthcare professional resp…
The terms of cooperation between the SAMU and the SMUR as well as the sectors and terms of intervention of the latter are specified in an agreement or in the network agreement mentioned in article R.…
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