Article R5121-42
The Director General of the Agence nationale de sécurité du médicament et des produits de santé shall refuse the marketing authorisation on the grounds mentioned in Article L. 5121-9. The application…
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Showing 5811–5820 of 22749 articles for “Art. Cass. com. 15 March 2011”
The Director General of the Agence nationale de sécurité du médicament et des produits de santé shall refuse the marketing authorisation on the grounds mentioned in Article L. 5121-9. The application…
The presentation at scientific or technical meetings, exhibitions and demonstrations of in vitro diagnostic medical devices which do not comply with the provisions of this Title is authorised provided…
For a new device, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, at any time and for a period of two years following the declaration provided for…
The purpose of vigilance of in vitro diagnostic medical devices, known as reactovigilance, is to monitor incidents and risks of incidents as defined in 1° of article R. 5222-2. It is carried out on al…
…461 of 21 April 2006 L. 313-4 Order no. 2019-740 of 17 July 2019 L. 313-5 Order no. 2016-301 of 14 March 2016 L. 313-5-1 Order no. 2013-544 of 27 June 2013 L. 313-5-2 Act no. 2003-721 of 1 August 200…
…461 of 21 April 2006 L. 313-4 Order no. 2019-740 of 17 July 2019 L. 313-5 Order no. 2016-301 of 14 March 2016 L. 313-5-1 Order no. 2013-544 of 27 June 2013 L. 313-5-2 Act no. 2003-721 of 1 August 200…
…461 of 21 April 2006 L. 313-4 Order no. 2019-740 of 17 July 2019 L. 313-5 Order no. 2016-301 of 14 March 2016 L. 313-5-1 Order no. 2013-544 of 27 June 2013 L. 313-5-2 Act no. 2003-721 of 1 August 200…
…ests for expert appraisal, under the conditions laid down in Section 6 of Chapter IV of this Title; 15° At least every two years, it submits to the Board of Directors an observation report on the prac…
…ed contribution for the year preceding the year of taxation exceeds €1,500 must pay:- no later than 15 June of the year of taxation, a first instalment equal to 50% of the business value added contrib…
…tions and minimum procedures provided for in the Annex to Commission Implementing Regulation (EU) 2015/1502 of 8 September 2015 laying down the technical specifications and minimum procedures relating…
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