Article R5121-29
…ollowing cases: 1° Its dossier is a simple duplicate of the marketing authorisation dossier for the reference medicinal product, and the pharmaceutical manufacturing establishment, the manufacturing p…
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Showing 871–880 of 14202 articles for “Art. Warrant mechanics reference”
…ollowing cases: 1° Its dossier is a simple duplicate of the marketing authorisation dossier for the reference medicinal product, and the pharmaceutical manufacturing establishment, the manufacturing p…
…ole president, sitting as a single judge. However, this judge may, if the complexity of the case so warrants, decide of his or her own motion or at the request of the convicted person or the public pr…
…or the application of this book in Saint-Pierre-et-Miquelon, in Articles L. 552-6 and L. 552-7, the reference to Regulation (EU) 2016/679 of 27 April 2016 on the protection of individuals with regard…
…I of Title III of Book IV. For the application of these provisions to Saint-Pierre-et-Miquelon, the reference to departments and regions is replaced by the reference to the territorial collectivity of…
…lemy, Saint-Martin and Saint-Pierre-et-Miquelon, subject to the adaptations in the present book :1° References to the provisions of the General Tax Code, the Book of Tax Procedures, the Customs Code a…
I. - When it orders the transfer of part of the assets, rights and obligations of a person subject to resolution proceedings to another entity or when it implements a measure provided for in II of Art…
For each reference work, the sum representing the automatic financial assistance calculated is obtained by multiplying the value of the minute point by its weighted duration.
…aging in any other behaviour that results in the manipulation of the calculation of such an index.A reference index is any publicly available or published rate, index or number that is determined peri…
…publisher or by a publisher of on-demand audiovisual media services, may be included on the list of reference works mentioned in article 311-28 drawn up in 2021, provided that the following conditions…
…y not be marketed until ten years have elapsed following the initial marketing authorisation of the reference medicinal product. However, this period is extended to eleven years if, during the first e…
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