Article Annexe XIII
PRINCIPAL CONTROL OPERATIONS WITH A VIEW TO CONTROLLING THE FIGURED CHARACTERISTICS OF TRADE EVENTS (Annex XIII of Annex 7-10 of Book Seven of the Decree section of the French Commercial Code) I. - Ge…
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Showing 3631–3640 of 8936 articles for “Art. 9 Mar 2004”
PRINCIPAL CONTROL OPERATIONS WITH A VIEW TO CONTROLLING THE FIGURED CHARACTERISTICS OF TRADE EVENTS (Annex XIII of Annex 7-10 of Book Seven of the Decree section of the French Commercial Code) I. - Ge…
…nal, responses are mandatory to enable your request to be processed. The loi n° 78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés grants you the right to access and recti…
…al, responses are mandatory to enable your request to be processed. The Law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms grants you the right to access and rectif…
…al, responses are mandatory to enable your request to be processed. The Law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms grants you the right to access and rectif…
…al, responses are mandatory to enable your request to be processed. The Law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms grants you the right to access and rectif…
…al, responses are mandatory to enable your request to be processed. The Law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms grants you the right to access and rectif…
…al, responses are mandatory to enable your request to be processed. The Law no. 78-17 of 6 January 1978 relating to information technology, files and freedoms grants you the right to access and rectif…
The purpose of veterinary pharmacovigilance is to monitor the effects of veterinary medicinal products, mainly their adverse effects on animals and humans, and the scientific evaluation of information…
…ry medicinal product subject to parallel distribution is a proprietary medicinal product : 1° Has a marketing authorisation issued by the European Union pursuant to Regulation (EC) No 726/2004 of the…
Only medicinal products which have obtained a marketing authorisation issued by the European Union in application of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 Mar…
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