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Categories
Clinical Trials
Creative Writing
IT & Software
Probability & Statistics
Public Awareness
Research & Publication
Services
Search for:
Contact
About Us
Cart
0
Register
Login
Curriculum
4 Sections
11 Lessons
8 Weeks
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Module 1
1
1.1
Introduction to Clinical Trials.
Module 2
4
2.0
Prerequisite certifications and trainings for CRCs.
2.1
EDC, EMR and Databases.
2.2
SEV, SIV and Monitor Visits, CRC Focused.
2.3
CRC responsibilities and expectations
Module 3
5
3.0
Regulatory training and requirements
3.1
Regulatory binder and Patient folder preparation
3.2
Regulatory forms FDA 1572, FDF, Delegation log etc
3.3
AE and SAE reporting.
3.4
Protocol Deviation reporting.
Module 4
1
4.1
Patient Encounter and Common Case Scenarios for CRCs.
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