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Showing 7351–7360 of 16903 articles for “Art. CE 23-6-1986 n° 50655”
…egional Audit Chamber must formulate its opinion and, where appropriate, its proposals, begins on receipt at the Registry of all the documents referred to in the previous paragraph which must be produ…
For the application of article L. 6223-6, a medical biologist who works at least half-time in the medical biology laboratory is considered to be an employed or self-employed medical biologist if his w…
…es and former employees within the framework of company mutual funds governed by Chapter III of loi n° 88-1201 du 23 décembre 1988relative aux organismes de placement collectif en valeurs mobilières e…
The list of services whose rates are governed by Title IV bis (regulatory part) of the French Commercial Code is as follows:Table 1 annexed to Article R. 444-3\n\t\t\t\tJUDICIAL AUCTIONEER\n\t\t\t\t\n…
…n article L. 23-11-1 is set out in an agreement between any holder of securities and the company concerned, which undertakes to transfer the amount resulting from the sharing commitment to the employe…
All in vitro diagnostic medical devices imported, placed on the market or put into service must bear the CE mark. However, CE marking is not required for devices undergoing a performance evaluation or…
The affixing of marks or inscriptions on a medical device, on its packaging or on the instructions for use which are likely to mislead as to the meaning or form of the CE marking is prohibited. Any ot…
…6 are applicable to condom advertising. Applications for approval must be accompanied either by the certificate of conformity required by the regulations in force, or by proof that the CE marking prov…
…of 9 January 1986 as amended relating to the statutory provisions governing the hospital civil service are applicable to the contractual practitioner.
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
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