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Clinical Research in Oncology
Health Professionals
Q-CROC Academy
Webinars
Microlearning Capsules
Training Directory
Ethics
Good clinical practice
University training ($)
Reference Documents
Competency Development Tool
ICH E6(R2) Good Clinical Practice
ICH E8(R1) General Considerations for Clinical Trials
Talking to Your Patient About a Clinical Trial
Directory of professional services
Biostatistics
Translation
Regulatory Affairs
Training Services
Monitoring Services
Quality Management Systems, Audits and Electronic System Validation
Communities of Practice
Patients
Discover Clinical Research
Clinical trials
Who is concerned?
The decision to participate
Do I qualify?
Learn more about clinical trials
News
Menu
Health Professionals
Q-CROC Academy
Webinars
Microlearning Capsules
Training Directory
Ethics
Good clinical practice
University training ($)
Reference Documents
Competency Development Tool
ICH E6(R2) Good Clinical Practice
ICH E8(R1) General Considerations for Clinical Trials
Talking to Your Patient About a Clinical Trial
Directory of professional services
Biostatistics
Translation
Regulatory Affairs
Training Services
Monitoring Services
Quality Management Systems, Audits and Electronic System Validation
Communities of Practice
Patients
Discover Clinical Research
Clinical trials
Who is concerned?
The decision to participate
Do I qualify?
Learn more about clinical trials
News
Find a Clinical Trial
All training
Good Clinical Practice and Regulation
IRB/IEC Responsibilities & Informed Consent
Trainer : SCRS & TransCelerate
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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