Multi-Center Study Sample Clauses

Multi-Center Study. Institution agrees that if the Study is part of a multi- center study, Institution shall not publish the results of the Study prior to the first multi-center publication. 6.4
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Multi-Center Study. Notwithstanding anything to the contrary in this Section 10, as the Study is part of a multi-center clinical research study, no submission for publication or public disclosure by Institution will be made until after publication of the overall multi-center results. Institution will ensure that Investigator will comply with the aforementioned. After the first to occur of (i) publication of the multi-center results, (ii) notification by Sponsor that such a multi-center submission for publication is no longer planned, or (iii) the eighteen (18) month anniversary of the termination of the study at all participating centers, Institution or the assigned Investigator may publish or publicly present the Study Data, subject to Institution’s and Investigator’s compliance with Sections 10.1 and 10.2, above. This Section 10.3 survives termination of this Agreement. 10.3 Multicentrická studie. Bez ohledu na ustanovení v rozporu s tímto oddílem 10, jelikož tato Studie je součástí multicentrické klinické výzkumné studie, žádosti o publikaci nebo veřejné zpřístupnění mohou být podány Zdravotnickým zařízením až poté, co budou publikovány celkové výsledky multicentrické studie. Zdravotnické zařízení zajistí, že Zkoušející bude dodržovat výše uvedené. Zdravotnické zařízení nebo pověřený Zkoušející mohou publikovat nebo veřejně prezentovat Údaje ze Studie, za předpokladu dodržení podmínek uvedených v oddílech 10.1 a 10.2 výše, až poté, co nastane některá z následujících událostí: (i) zveřejnění multicentrických výsledků, (ii) oznámení Zadavatele, že podání k zveřejnění výsledků multicentrické studie již není plánováno, nebo (iii) uplynutí osmnácti (18) měsíců od ukončení Studie ve všech zúčastněných centrech. Tento oddíl 10.3 zůstává v platnosti i po ukončení platnosti této Smlouvy.
Multi-Center Study. In the event of a multi-center Study, Institution agrees that each site involved in the Study (each a “Study Site” and collectively “Study Sites”) shall enter into a written agreement with Institution regarding its participation in the Study. Institution and Investigator shall be solely responsible for the conduct of the Study at all Study Sites, and shall ensure that the Study Sites comply with the terms and conditions of this Agreement and all Applicable Laws. Upon request by Company, Institution and Investigator shall provide a list of participating sites and any updates thereto. Institution shall prepare the form of the agreement to be used with the Study Sites, which shall afford Company all rights as set forth in this Agreement.
Multi-Center Study. In the event of a multi-center Study, Institution agrees that each site involved in the Study (each a “Study Site” and collectively “Study Sites”) shall enter into a written agreement with Institution regarding such Study Site’s participation in the Study with Institution and Sponsor. Institution and Investigator shall be responsible for the conduct of the Study at all Study Sites, and shall ensure that the Study Sites comply with the terms and conditions of this Agreement and all Applicable Laws.
Multi-Center Study. Notwithstanding anything to the contrary in this Article 10, as the Study is part of a multi-center clinical research study, no submission for publication or public disclosure by Provider or Investigator will be made until after publication of the multi-center results. After the first to occur of

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  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

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