Disclosure by Institution/Principal Investigator Sample Clauses

Disclosure by Institution/Principal Investigator. The Institution/Principal Investigator shall have the right to include the Study title and any other information publicly available on any registry in which the Study is listed pursuant to Section 3.5, in any list of active or past clinical trials conducted by the Institution/Principal Investigator published on the Institution/Principal Investigator’s website or in an Institution/Principal Investigator print publication; provided, however, that no additional information, whether about the Study, the Investigational Drug, or the Sponsor, may be included. 7.5 Zverejnenie informácií inštitúciou/zodpovedným skúšajúcim. Inštitúcia/zodpovedný skúšajúci majú právo zahrnúť názov klinického skúšania a akékoľvek ďalšie verejne dostupné informácie v akomkoľvek registri, v ktorom je uvedené toto klinické skúšanie podľa časti 3.5, do akéhokoľvek zoznamu aktívnych alebo minulých klinických skúšaní vykonaných touto inštitúciou/zodpovedným skúšajúcim, ktorý je zverejnený na webových stránkach inštitúcie/zodpovedného skúšajúceho alebo v tlačenej publikácii inštitúcie/zodpovedného skúšajúceho; avšak za predpokladu, že nebudú zahrnuté žiadne ďalšie informácie, či už o klinickom skúšaní, skúšanom lieku alebo zadávateľovi.
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Disclosure by Institution/Principal Investigator. The Institution/Principal Investigator shall have the right to include the Study title and any other information publicly available on any registry in which the Study is listed pursuant to Section 3.5, in any list of active or past clinical trials conducted by the Institution/Principal Investigator published on the Institution/Principal Investigator’s website or in an Institution/Principal Investigator print publication; provided, however, that no additional information, whether about the Study, the Investigational Drug, or the Sponsor, may be included. 7.5 Zpřístupnění informací ze strany zdravotnického zařízení/hlavního zkoušejícího. Zdravotnické zařízení/hlavní zkoušející xxxx právo uvést název studie a jiné informace, které jsou veřejně k dispozici v jakémkoliv registru, v němž xx xxxxxx uvedena podle oddílu 3.5, v jakémkoliv seznamu aktivních nebo minulých klinických hodnocení prováděných zdravotnickým zařízením/hlavním zkoušejícím, který je zveřejňován na webových stránkách zdravotnického zařízení/hlavního zkoušejícího nebo v některé z tištěných publikací zdravotnického zařízení/hlavního zkoušejícího, ovšem z a předpokladu, že nebudou uvedeny žádné další informace o studii, hodnoceném léčivu či o zadavateli.
Disclosure by Institution/Principal Investigator. The Institution /Principal Investigator shall have the right to include the Study title and any other information publicly available on any registry in which the Study is listed pursuant to Section 0, in any list of active or past clinical trials conducted by the Institution/Principal Investigator published on the Institution/Principal Investigator’s website or in an Institution/Principal Investigator print publication; provided, however, that no additional information, whether about the Study, the Investigational odkladu (s výhradou dalších oddílů tohoto článku 7). 7.3

Related to Disclosure by Institution/Principal Investigator

  • Principal Investigator The research will be under the direction of (“Principal Investigator”). If, for any reason, he/she is unable to continue to serve as Principal Investigator and a successor acceptable to both UHD and Sponsor is not available, this Agreement shall be terminated as provided in Section 7.

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  • Institution and Investigator acknowledge that SPONSOR has no obligation to indemnify or be responsible for any loss, claim, cost (including reasonable attorney fees) or demand if and to the extent such losses, claims or demands arise from any injuries or damages resulting from Institution’s, Investigator’s or the Study Personnel’s negligence, breach of this Agreement, failure to adhere to the Protocol, failure to obtain signed informed consent forms, failure to follow Applicable Law, misuse of the Study Drug, unauthorized warranties, or willful misconduct. This indemnification obligation is without prejudice to the precedence of insurance coverage from compulsory clinical trial insurance. 12.3. Zdravotnické zařízení a zkoušející berou na vědomí, že ZADAVATEL nevyplatí žádné odškodnění ani není odpovědný za žádné ztráty, náklady, spory (včetně přiměřených nákladů na právní pomoc) či nároky v souvislosti s újmou či škodou, ke kterým došlo v důsledku nedbalosti na straně zdravotnického zařízení, zkoušejícího a/nebo členů týmu provádějícího klinické hodnocení a/nebo v důsledku toho, že zdravotnické zařízení, zkoušející a/nebo některý člen týmu provádějícího klinické hodnocení porušili ustanovení této smlouvy, porušili ustanovení protokolu, nenechali subjekt hodnocení podepsat informovaný souhlas, porušili ustanovení platných zákonů, chybným způsobem použili studijní léčivo ZADAVATELe, způsobili škodu úmyslným zaviněním a/nebo poskytli neoprávněné záruky. Touto povinností odškodnění není dotčeno přednostní pojistné krytí z povinného pojištění klinického hodnocení.

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  • Teachers with Principal Designations (Effective October 22, 2019, the following repeals and replaces clause 4.4. above)

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