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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
Essential Documents for a Clinical Study
Trainer : SCRS & TransCelerate
Describes the requirements for Clinical Study essential documents. Describes the type of essential documents collected for a Clinical Study during the different study phases.
Link to training
English
20 Minutes
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