Close
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 ($)
Directory of professional services
Biostatistics
Translation
Regulatory Affairs
Monitoring services (CRA)
Training Services
Quality Management Systems, Audits and Electronic System Validation
Communities of Practice
Patients
Discover Clinical Research
Frequently asked questions
Learn more about clinical trials
News
Who We Are
Our Members
Our Team
Governance
Privacy Policy
Careers
Contact
Français
Who We Are
Our Members
Our Team
Governance
Privacy Policy
Careers
Contact
Français
Search
Clinical Research in Oncology
Professionals
Q-CROC Academy
Webinars
Microlearning Capsules
Reference Documents
Competency Development Tool
ICH E6(R2) Good Clinical Practice
ICH E8(R1) General Considerations for Clinical Trials
Site Resource for Invoiceables
Talking to Your Patient About a Clinical Trial
Training Directory
Ethics
Good clinical practices
University training ($)
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
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
Source Documentation
Trainer : SCRS
A review of the terms source data and source documents. Describes the key attributes of source documents, the intent of ALCOA and CCEA and describes the appropriate processes for creating, maintaining and storing source documents.
Link to training
English
20 Minutes
Prev
Previous
Delegation and Training
Next
Essential Documents for a Clinical Study
Next
Back to top