Common use of Duties of Investigator Investigator Clause in Contracts

Duties of Investigator Investigator. is responsible for the conduct of the Study at Institution. This Agreement does not cover the arrangements made between Sponsor, IQVIA and Investigator concerning the conduct of the Study by the Investigator. These arrangements, including payments due to the Investigator for performance of the Study, are detailed in a separate written agreement. In particular, but without limitation, it is the Investigator’s duty to review and understand the information in the Investigator’s Brochure or device labeling instructions. IQVIA or Sponsor will ensure that all required reviews and approvals by applicable regulatory authorities and ECs are obtained. Institution acknowledges that the Investigator is responsible prior to commencement of the study to ensure that all approvals by applicable regulatory authorities and ECs have been obtained and to to review all CRFs to ensure their accuracy and completeness. Institution acknowledges that Investigator shall 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. Investigator acknowledges that he/she shall 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. není v této souvislosti vyžadováno během takových kontrol. V případě jakýchkoli připomínek úřadů nebo Zadavatele na základě jakéhokoli sledování a inspekcí Poskytovatel zdravotních služeb bez zbytečného odkladu provede veškerá opatření k nápravě podle pokynů úřadů, IQVIA a/nebo Zadavatele.

Duties of Investigator Investigator. is responsible for the conduct of the Study at Institution. This Agreement does not cover the arrangements made between Sponsor, IQVIA and Investigator concerning the conduct of the Study by the Investigator. These arrangements, including payments due to the Investigator for performance of the Study, are detailed in a separate written agreement. In particular, but without limitation, it is the Investigator’s duty to review and understand the information in the Investigator’s Brochure or device labeling instructions. IQVIA or Sponsor will ensure that all required reviews and approvals by applicable regulatory authorities and ECs are obtained. Institution acknowledges that the The Investigator is responsible prior to commencement of the study to ensure that all approvals by applicable regulatory authorities and ECs have been obtained and to to review all CRFs to ensure their accuracy and completeness. Institution acknowledges that Investigator shall 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. Investigator acknowledges that he/she shall 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. za účelem oddělení, nikoli však odhalení či zpřístupnění, veškerých Důvěrných informací, jejichž odhalení či zpřístupnění není v této souvislosti vyžadováno během takových kontrol. Uvedenými povinnostmi je Zdravotnické zařízení vázáno pouze v případě, že jejich splnění nebudou bránit platné právní předpisy či rozhodnutí nebo jiné opatření regulatorního orgánu. V případě jakýchkoli připomínek úřadů nebo Zadavatele na základě jakéhokoli sledování a inspekcí Poskytovatel zdravotních služeb bez zbytečného odkladu Zdravotnické zařízení okamžitě provede veškerá opatření k nápravě podle pokynů úřadů, IQVIA a/nebo Zadavatele.

Duties of Investigator Investigator. is responsible for the conduct of the Study at Institution. This Agreement does not cover the arrangements made between Sponsor, IQVIA and Investigator concerning the conduct of the Study by the Investigator. These arrangements, including payments due to the Investigator for performance of the Study, are detailed in a separate written agreement. In particular, but without limitation, it is the Investigator’s duty to review and understand the information in the Investigator’s Brochure or device labeling instructions. IQVIA or Sponsor will ensure willensure that all required reviews and approvals by applicable regulatory authorities and ECs are obtained. Institution acknowledges that the The Investigator is responsible prior to commencement of the study to ensure that all approvals by applicable regulatory authorities and ECs have been obtained and to to review all CRFs to ensure their accuracy and completeness. Institution acknowledges that Investigator shall provide a written declaration revealing Investigator’s possible economic or other interestske Studii, if anyzejména včetně žádostí či oznámení o kontrole prostor a zařízení Zdravotnického zařízení, in connection with the conduct of the Study or the Investigational Producta Zdravotnické zařízení umožní společnosti IQVIA a Zadavateli, aby se takových kontrol zúčastnili. Investigator acknowledges that he/she shall provide a written declaration revealing Investigator’s disclosure obligationsZdravotnické zařízení vyvine nezbytné úsilí za účelem oddělení, if anynikoli však odhalení či zpřístupnění, with the Institution in connection with the conduct of the Study and the Investigational Product. veškerých Důvěrných informací, jejichž odhalení či zpřístupnění není v této souvislosti vyžadováno během takových kontrol. V případě jakýchkoli připomínek úřadů nebo Zadavatele na základě jakéhokoli sledování a inspekcí Poskytovatel zdravotních služeb bez zbytečného odkladu provede veškerá opatření k nápravě podle pokynů úřadů, IQVIA a/nebo Zadavatele.

Duties of Investigator Investigator. is responsible for the conduct of the Study at Institution. This Agreement does not cover the arrangements made between Sponsor, IQVIA and Investigator concerning the conduct of the Study by the Investigator. These arrangements, including payments due to the Investigator for performance of the Study, are detailed in a separate written agreement. In particular, but without limitation, it is the Investigator’s duty to review and understand the information in the Investigator’s Brochure or device labeling instructionsBrochure. IQVIA or Sponsor will ensure willensure that all required reviews and approvals by applicable regulatory authorities and ECs are obtained. Institution acknowledges that the Investigator is responsible prior to commencement of the study to ensure that all approvals by applicable regulatory authorities and ECs have been obtained and to to review all CRFs to ensure their accuracy and completeness. Institution acknowledges that agrees to provide advance notice to Sponsor and IQVIA if Investigator shall provide a written declaration revealing Investigator’s possible economic or other interests, if any, will be terminating its employment relationship in connection with the conduct of the Study or the Investigational Product. Investigator acknowledges that he/she shall 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 Productor is otherwise no longer able to perform prostor a zařízení Poskytovatele zdravotních služeb, a Poskytovatel zdravotních služebumožní IQVIA a Zadavateli, aby se takových kontrol zúčastnili. Poskytovatel zdravotních služebvyvine nezbytné úsilí za účelem oddělení, nikoli však odhalení či zpřístupnění, veškerých Důvěrných informací, jejichž odhalení či zpřístupnění není v této souvislosti vyžadováno během takových kontrol. V případě jakýchkoli připomínek úřadů nebo Zadavatele na základě jakéhokoli sledování a inspekcí Poskytovatel zdravotních služeb bez zbytečného odkladu provede veškerá opatření k nápravě podle pokynů úřadů, IQVIA a/nebo Zadavatele.