CNRS Sample Clauses

CNRS. As to CNRS, it is agreed between the Beneficiaries that, to the best of their knowledge, the following Background is hereby identified and agreed upon for the Project. Background of the CNRS is, all Know-how generated within the researches of: Xxxxx XXXXXXXXXX at the CNRS-LJAD (UMR7351) as far as needed to duly perform our work in the Project; items of CNRS-ICSM identified in the table below. Describe Background Specific limitations and/or conditions for implementation Specific limitations and/or conditions for exploitation CNRS-LJAD hereby includes Access Rights to all Background that has been created by the Research headed by Xxxxx Xxxxxxxxxx and that is specifically needed for the implementation of the EURAD (GA N0 847593) project. N/A N/A CNRS-LJAD : Models and algorithms for the coupling of Xxxxx and free flows as described in the following articles : L. Beaude, X. Xxxxxxx, X. Xxxxx, X. Xxxxxx, F. Smai, Non-isothermal compositional Xxxxx flows: formulation, soil-atmosphere boundary condition and application to high energy geothermal simulations, Computational Geosciences, online 3 dec. 2018. N. Birgle, X. Xxxxxx, X. Xxxxxx, A domain decomposition method to couple nonisothermal compositional gas liquid Xxxxx and free gas flows, Journal of Computational Physics, 368, 1, pp. 210–235, 2018. X. Xxxxxx, X. Xxxxxx, X. Xxxxx, Coupling compositional gas liquid and free gas flow at porous and free flow domains interface. Journal of Computational Physics, 15 september, 321, pp. 708–728, 2016. X. Xxxxxx, L. Trenty, X. Xxxxx, Coupling of a two phase gas liquid compositional 3D Xxxxx flow with a 1D compositional free gas flow. M2AN, 50, 5, 2016. N/A N/A CNRS-LJAD : Open source code ComPASS xxxx://xxx.xxx- xxxxxx.xxx/xxxx/xxxxxxx-xxxx distribué sous la licence GPL/CeCILL v2.1 N/A N/A CNRS-ICSM: Preparation of UO2 samples containing fission products, for which synthesis methods have been optimized (oxalate conversion, hydroxide conversion) N/A N/A CNRS-ICSM : Multiparametric study of the dissolution (microscopic-macroscopic dual approach) in the field of the development of fuel reprocessing activities N/A N/A This represents the status at the time of signature of this Consortium Agreement.
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Related to CNRS

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  • Povinnosti Zkoušejícího Investigator is responsible for the conduct of the Study at Institution. In particular, but without limitation, it is the Investigator’s duty to review and understand the information in the Investigator’s Brochure to ensure that all informed consent requirements are followed. IQVIA or Sponsor will ensure that all required reviews and approvals by applicable regulatory authorities and ECs are obtained. Zkoušející je odpovědný za provedení Studie ve Zdravotnickém zařízení. Konkrétně pak jde zejména, ale nejen o povinnost Zkoušejícího zkontrolovat a porozumět informacím obsaženým v Souboru informací pro zkoušejícího a zajistit dodržování všech požadavků týkajících se informovaného souhlasu. IQVIA nebo Zadavatel zajistí, že budou opatřena veškerá požadovaná kontrolní schválení od příslušných regulatorních úřadů a EK. Investigator agrees to provide a written declaration revealing Investigator’s possible economic or other interests, if any, in connection with the conduct of the Study or the Investigational Product, or the Sponsor. Zkoušející souhlasí, že poskytne písemné prohlášení vztahující se k potenciálním zájmům Zkoušejícího ekonomické či jiné povahy, či odhalí jiné zájmy, je-li jich, a to v souvislosti s prováděním této Studie či ve vztahu k Hodnocenému léčivu i ve vztahu k Zadavateli. Investigator agrees to provide a written declaration revealing Investigator’s disclosure obligations, if any, with the Institution in connection with the conduct of the Study and the Investigational Product. Zkoušející souhlasí, že poskytne písemné prohlášení, jež bude odhalovat závazky Zkoušejícího, jsou-li nějaké, a to vůči Zdravotnickému zařízení ve vztahu a v souvislosti s prováděním Studie a Hodnoceným léčivem. Investigator is duly licensed to conduct the Study and in good standing. Zkoušející má řádné a platné příslušné oprávnění k provádění Studie. Site agrees to provide prompt advance notice to Sponsor and IQVIA if Investigator will be terminating its employment relationship in the Institution or is otherwise no longer able to perform the Study. The appointment of a new Investigator must have the prior approval of Sponsor and IQVIA. Místo provádění klinického hodnocení souhlasí, že zašle předem promptní oznámení Zadavateli a IQVIA v případě, že Zkoušející ukončí pracovní poměr ve Zdravotnickém zařízení či nebude-li Zkoušející z jakéhokoli jiného důvodu schopen provádět Studii. Ustanovení nového Zkoušejícího bude podléhat předchozímu schválení Zadavatele a IQVIA.

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