Study Registration Clause Samples
Study Registration. Sponsor will register the Study with the public clinical trials registry ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ in accordance with Applicable Laws and Requirements and ICMJE guidelines prior to the enrolment of the first Subject. Where Institution and Principal Investigator wish to use a publicly-accessible website on a voluntary basis (e.g., a university/hospital website) the information related to the Protocol must not exceed the information Sponsor has already posted and it should be sufficient to provide a hyperlink to the trial when registered on ▇▇▇▇://▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇/ 9.3 Registrace Studie: Před zařazením prvního Subjektu Zadavatel zaregistruje Studii ve veřejném registru klinických hodnocení ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ v souladu s Platnými právními předpisy a požadavky a pokyny ICMJE. Bude-li si Zdravotnické zařízení a Hlavní zkoušející přát dobrovolně využít veřejně dostupné webové stránky (např. webové stránky univerzity / nemocnice), nesmí informace týkající se Protokolu přesahovat informace, které Zadavatel již zveřejnil, a po zaregistrování na stránkách ▇▇▇▇://▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ by mělo být postačující uvést hypertextový odkaz na tyto stránky.
Study Registration. Sponsor will register the Study with the public clinical trials registry ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ in accordance with Applicable Laws and Requirements and ICMJE guidelines prior to the enrolment of the first Subject. Where Institution and Principal Investigator wish to use a publicly-accessible website on a voluntary basis (e.g., a university/hospital website) the information related to the Protocol must not exceed the information Sponsor has already posted and it should be sufficient to provide a hyperlink to the trial when registered on ▇▇▇▇://▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇/.
Study Registration. Pfizer encourages Institution and Principal Investigator to register the Study and any synopsis of Study Results on ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or such other website as required under Applicable Law before enrollment of the first Study subject or before commencement of data collection.
Study Registration. Abbott shall register Studies at either ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or any other registry as applicable or required by law and consistent with the guidelines of the International Committee of Medical Journal Editors (“ICMJE”) on trial registrations.
Study Registration. RedHill agrees to register the Study at either ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or any other registry as applicable or required by law and consistent with the guidelines of the International Committee of Medical Journal Editors on trial registrations.
Study Registration. ▇▇▇▇▇▇ shall register Studies at either ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or any other registry as applicable or required by law and consistent with the guidelines of the International Committee of Medical Journal Editors (“ICMJE”) on trial registrations. 4.5
Study Registration. Pfizer encourages Institution to register the Study and post a synopsis of Study Results on ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ or other website as required by Applicable Law. 3. INVESTIGATOR-SPONSORED RESEARCH SUPPORT 3.1. ISR Support. Pfizer will provide funding in support of the Study up to a maximum amount of CZK [XXXX], in accordance with the schedule set forth in Attachment A (“ISR Support”). Pfizer will provide the ISR Support only to Institution. Institution is responsible for appropriate dispersal of funds to Participating Sites. Pfizer will not provide the Pfizer Product that is the focus of this non-interventional Study. Study subjects received the Pfizer Product by prescription as part of their standard medical care. 3.
Study Registration. The Principal Investigator (PI) will register the study on CTRI and the registration number would be provided to them once available.