Obligations of the Investigator. Research Staff, and Institution Data Files provided under this Agreement shall be held by the Investigator, Research Staff, and Institution in confidence and can be disclosed only in compliance with the terms of this Agreement. In consideration of the promises contained in Section IV of this agreement, and for use of Data Files from Add Health, the Investigator and Research Staff, as employees or agents of the Institution, shall abide by the terms of this Agreement, and the Institution agrees:
Obligations of the Investigator. 2.1 The Investigator shall at all times be responsible for the direction and performance of the Study at the Study Site.
Obligations of the Investigator. 1. Protocol 1.1.Investigator shall conduct the clinical trial, with CRO’s oversight, in accordance with the Protocol, the applicable Regulations and the terms and conditions of this Agreement. The clinical trial will be conducted according to the conditions specified under applicable Regulations. 1.2.If applicable under the local legal framework, the Investigator shall submit to SPONSOR/CRO and then to Institutional V. Povinnosti zkoušejícího 1. Protokol 1.1.Zkoušející povede klinické hodnocení s dozorem CRO, dle Protokolu, odpovídajících Předpisů a nařízení dle této Smlouvy. Klinické hodnocení bude prováděno dle podmínek specifikovaných v odpovídajících Předpisech 1.2.Zkoušející předloží Zadavateli/CRO a poté Instituonal Review Board (IRB)/Nezávislé etické komisi (IEC) k předchozímu
Obligations of the Investigator. Research Staff, and Institution Restricted Data provided under this Agreement shall be held by the Investigator, Research Staff, and Institution in strictest confidence and can be used or disclosed only in compliance with the terms of this Agreement. In consideration of the promises in Section V of this Agreement, and for use of Restricted Data from ICPSR, the Institution agrees:
Obligations of the Investigator. 3.1 Investigator agrees to use the Equipment only for the purpose of conducting the Trial and in a manner adequate to the nature and qualification of the Equipment as well as in accordance with the purpose it serves.
Obligations of the Investigator. 3.1 Investigator agrees to use the Equipment only for the purpose of conducting the Trial and in a manner adequate to the nature and qualification of the Equipment as well as in accordance with the purpose it serves. 3.2 Investigator shall (i) use the Equipment in accordance with operating instructions/manuals provided as well as all applicable laws, regulations, and guidelines; (ii) in the course of the handover of the Equipment and before its use, examine the 3. POVINNOSTI ZKOUŠEJÍCÍHO 3.1 Zkoušející se zavazuje užívat Zařízení pouze pro účely provádění Klinického hodnocení a způsobem přiměřeným povaze a kvalifikaci Zařízení a v souladu s účelem, jemuž slouží. 3.2
