Common Contracts

2 similar Chief Investigator Agreement contracts

Roles & Responsibilities of Chief Investigator Agreement
Chief Investigator Agreement • July 1st, 2020

The Chief Investigator (CI) and all members of the research team shall comply with all current regulations (as amended from time to time) applicable to the performance of the study including, but not limited to:  Policy Framework for Health & Social Care or relevant Governance Framework The Principles of the World Medical Association Declaration of Helsinki Data Protection Act (1998/2018) General Data Protection Regulations (2018) ICH Good Clinical Practice Guidelines (1996) and Revision 2 (R2 2017) Human Tissue Act (2006) UK Medicines for Human Use (Clinical Trials) Regulations (2004) UK Medicines for Human Use (Clinical Trials) Amendment Regulations 2006, SI 2006/1928 The UK Medicines for Human Use (Clinical Trials) Amendment (No.2) Regulations 2006, SI 2006/2984 The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008, SI 2008/941 The Mental Capacity Act (2005) I confirm that I have read and understood my responsibilities as

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Roles & Responsibilities of Chief Investigator Agreement
Chief Investigator Agreement • July 1st, 2020

The Chief Investigator (CI) and all members of the research team shall comply with all current regulations (as amended from time to time) applicable to the performance of the study including, but not limited to:  Policy Framework for Health & Social Care or relevant Governance Framework The Principles of the World Medical Association Declaration of Helsinki Data Protection Act (1998/2018) General Data Protection Regulations (2018) ICH Good Clinical Practice Guidelines (1996) and Revision 2 (R2 2017) Human Tissue Act (2006) UK Medicines for Human Use (Clinical Trials) Regulations (2004) UK Medicines for Human Use (Clinical Trials) Amendment Regulations 2006, SI 2006/1928 The UK Medicines for Human Use (Clinical Trials) Amendment (No.2) Regulations 2006, SI 2006/2984 The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008, SI 2008/941 The Mental Capacity Act (2005) I confirm that I have read and understood my responsibilities as

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