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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
Source Documentation
Trainer : SCRS & TransCelerate
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
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Delegation and Training
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Essential Documents for a Clinical Study
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