Article R910-2
For the application of this code in Saint-Pierre-et-Miquelon, the terms listed below are replaced as follows:1° "Tribunal judiciaire" by "tribunal de première instance";2° "Cour d'appel" by "tribunal…
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Showing 2411–2420 of 8432 articles for “Art. CJEU – Pierre Fabre – 13 Oct. 2011 – C-439/09”
For the application of this code in Saint-Pierre-et-Miquelon, the terms listed below are replaced as follows:1° "Tribunal judiciaire" by "tribunal de première instance";2° "Cour d'appel" by "tribunal…
The following provisions shall not apply in Saint-Pierre-et-Miquelon:1° Articles R. 123-209 to R. 123-219, D. 145-12 to D. 145-19, D. 146-1 and D. 146-2;2° Articles R. 229-1 to R. 229-26 and R. 252-1…
References to provisions of the General Tax Code are replaced by locally applicable tax law provisions.
In the absence of adaptation, references made by provisions of this code applicable to Saint-Pierre-et-Miquelon, to provisions that do not apply there, are replaced by references to provisions with th…
Articles referring to the European Community shall apply in compliance with the Association Decision provided for in Article 187 of the Treaty establishing the European Community. References to the Ag…
References made, by provisions of this code applicable to Saint-Pierre-et-Miquelon, to other articles of this code, concern only those articles made applicable in the collectivity with the adaptations…
…e rules in force in mainland France pursuant to that Directive. VII. - The reference to Directive 2013/34/EU of the European Parliament and of the Council of 26 June 2013 on the annual financial state…
…ucts in article R. 5121-172 ;3° For the homeopathic medicinal products mentioned in article L. 5121-13, after the registration provided for in that article;4° For the traditional herbal medicinal prod…
…ct mentioned in Article R. 5121-150 concerning one or more of these medicinal products or products; 13° "Medication error": an unintentional error by a healthcare professional, a patient or a third pa…
Pharmacovigilance includes: 1° The reporting of adverse reactions suspected to be due to a medicinal product or a product mentioned in article R. 5121-150, including cases of overdose, misuse, abuse a…
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