ZDRAVOTNICKÉ ZAŘÍZENÍ A ZKOUŠEJÍCÍ. Institution shall provide all personnel, facilities and other resources required to conduct and complete the Clinical Trial in a timely and professional manner and according to the terms of this Agreement, unless expressly provided in Appendix 1. Institution shall only use sub-investigators, nurses and other personnel for the conduct of the Clinical Trial (the “Clinical Trial Staff”) who can document that they are qualified as well as trained in accordance with ICH GCP. Institution is responsible for ensuring that the Clinical Trial Staff comply with the terms of this Agreement and the Protocol. The delegation of any task of Investigator to any Clinical Trial Staff must be documented in writing prior to the implementation of the delegation. 2.
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Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
ZDRAVOTNICKÉ ZAŘÍZENÍ A ZKOUŠEJÍCÍ. Institution shall provide all personnel, facilities and other resources required to conduct and complete the Clinical Trial in a timely and professional manner and according to the terms of this Agreement, unless expressly provided in Appendix 1. Institution and Investigator shall only use sub-sub- investigators, nurses and other personnel for the conduct of the Clinical Trial (the “Clinical Trial Staff”) who can document that they are qualified as well as trained in accordance with ICH GCP. Institution is and Investigator are responsible for ensuring that the Clinical Trial Staff comply with the terms of this Agreement and the Protocol. The delegation of any task of Investigator to any Clinical Trial Staff must be documented in writing prior to the implementation of the delegation. 2.
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