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Clinical Research in Oncology
Professionals
Q-CROC Academy
Webinars
Microlearning Capsules
Reference Documents
Competency Development Tool
ICH E6(R2) Good Clinical Practice
ICH E8(R1) General Considerations for Clinical Trials
Site Resource for Invoiceables
Talking to Your Patient About a Clinical Trial
Training Directory
Ethics
Good clinical practices
University training ($)
Directory of professional services
Biostatistics
Translation
Regulatory Affairs
Monitoring services (CRA)
Training Services
Quality Management Systems, Audits and Electronic System Validation
Communities of Practice
Patients
Discover Clinical Research
Frequently asked questions
Learn more about clinical trials
News
Menu
Professionals
Q-CROC Academy
Webinars
Microlearning Capsules
Reference Documents
Competency Development Tool
ICH E6(R2) Good Clinical Practice
ICH E8(R1) General Considerations for Clinical Trials
Site Resource for Invoiceables
Talking to Your Patient About a Clinical Trial
Training Directory
Ethics
Good clinical practices
University training ($)
Directory of professional services
Biostatistics
Translation
Regulatory Affairs
Monitoring services (CRA)
Training Services
Quality Management Systems, Audits and Electronic System Validation
Communities of Practice
Patients
Discover Clinical Research
Frequently asked questions
Learn more about clinical trials
News
OncoQuébec
All training
Good Clinical Practice
IRB/IEC Responsibilities & Informed Consent
Trainer : SCRS
Overview of the purpose and activities of the IRB/IEC and the Investigator’s responsibilities in accordance with ICH-GCP. Describes the process of informed consent and the responsibilities of the Investigator when obtaining informed consent.
Link to training
English
30 Minutes
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