Institution and Principal Investigator Sample Clauses

Institution and Principal Investigator. 1.1 The Institution and the Principal Investigator (or Responsible Technical Officer), who must be an employee of the Institution, shall be jointly responsible for all the technical and administrative aspects of the work referred to in this Agreement. 1.2 The Institution is required to notify WHO immediately of knowledge that the Principal Investigator will cease or ceases to be an employee of the Institution or is no longer continuing the responsibilities covered by this Agreement. Under such circumstances WHO has the right to: a. cancel this Agreement or b. agree to continue the project under a new Principal Investigator proposed by the Institution and approved by WHO.
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Institution and Principal Investigator understand and agree that this Agreement is being signed by CRO in its own name as a contracting party receiving services under this Agreement and in addition, in a separate capacity, CRO also signs this Agreement in the name of Janssen and for Janssen’s benefit.
Institution and Principal Investigator agree to fully cooperate with respect to any data protection impact assessments and/or prior consultations that may be required with respect to the processing of Personal Information under the Agreement.
Institution and Principal Investigator. The Institution of this Study is: CheckBox6 Taipei Medical University Hospital CheckBox6 Taipei Municipal Wanfang Hospital CheckBox6 Taipei Medical University-Xxxxxx Xx Hospital, Ministry of Health and Welfare
Institution and Principal Investigator agree not to use Confidential Information for any purposes other than to conduct the Study. Institution and Principal Investigator agree not to disclose Confidential Information to third parties except as necessary to conduct the Study and under an agreement by the third party to be bound by the obligations of this section. Institution and Principal Investigator shall safeguard Confidential Information with the same standard of care that is used with Institution’s Confidential Information, but in no event less than reasonable care.
Institution and Principal Investigator shall comply and shall require any of the persons or entities performing the Services on their behalf to comply, with all applicable laws, rules, regulations, and guidelines governing the privacy of personally identifiable information and patient health information in Xxxxx Xxxxxxxx.
Institution and Principal Investigator being the sponsor, agree that neither COMPANY, nor any of its affiliates or subsidiaries, their respective officers, directors, employees, contractors or agents will bear any responsibility or liability for claims, losses, injuries, or other damages, including any consequential, incidental, special, or indirect damages (including loss of profits or business opportunity), to the extent that any of the above arises from: (i) any breach of this Agreement by INSTITUTION or PRINCIPAL INVESTIGATOR or by any of the clinical staff involved in the Study, including any failure to comply with the terms of the Study Protocol or any deviation of the study protocol or the Company’s written instructions with respect to the performance of the Study and/or use or administration of the Study Product; (ii) the failure by INSTITUTION, PRINCIPAL INVESTIGATOR and/or any of the clinical staff involved in the Study and/or any agents or contractors of Institution involved in the performance of the Study to comply with any applicable law, regulations, guidelines or other governmental requirements; (iii) the negligent, reckless or wrongful act, error or omission, willful misconduct or bad faith of INSTITUTION, PRINCIPAL INVESTIGATOR and/or any clinical staff and/or any agents or contractors of Institution involved in the performance of the Study; or (iv) any bodily injury to a third party (including a Study Subject) caused by act or omission of the INSTITUTION, PRINCIPAL INVESTIGATOR or the clinical stuff involved in the Study, and INSTITUTION and PRINCIPAL INVESTIGATOR will indemnify, defend, and hold COMPANY harmless and its respective subsidiaries and affiliates, and their respective officers, directors , employees, contractors and agents harmless from such liability. INSTITUTION and PRINCIPAL INVESTIGATOR shall not settle or compromise any claim for which COMPANY is indemnified without the prior written consent of COMPANY. COMPANY shall have no obligation of indemnification hereunder for any loss or damages arising out of the negligence or willful misconduct or failure to act of PRINCIPAL INVESTIGATOR, INSTITUTION, their officers, agents, and/or employees in connection with the conduct of the Study.
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Institution and Principal Investigator agree to and shall defend, indemnify and hold Radiometer and its employees harmless from and against any injury to persons or damage to property, to the extent that such injury or damage is caused by or arises out of the negligence or the reckless or intentional misconduct of Institution and Principal Investigator or its directors, trustees, employees or staff in carrying out the Study.
Institution and Principal Investigator. 1 ROZSAHPRACÍ 1.1 Zdravotnické zařízení a hlavní zkoušející budou provádět studii ve zdravotnickém zařízení, a to v přísném souladu s podmínkami této smlouvy, jakýmikoliv písemnými pokyny zadavatele a/nebo společnosti Medpace, všemi obecně přijímanými standardy správné klinické praxe, protokolem a všemi platnými místními zákony a předpisy upravujícími provádění klinického výzkumu. Místo provádění studie nebude měněno bez předchozího písemného souhlasu společnosti Medpace.
Institution and Principal Investigator shall indemnify, defend and hold harmless PPD and GSK and its Affiliates from any and all losses, injuries, harm, costs or expenses, including without limitation, reasonable attorney's fees, incurred by PPD or GSK or its Affiliates as a result of the negligence or willful misconduct of Institution and/or Principal Investigator.
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