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CRA + CRC Certification Program: Clinical Trial Conduct & Monitoring
1 Module I – Introduction to Clinical Research *
2 Module II – Essentials of ICH GCP & FDA regulations
3 Module III – Basics of Clinical Trials Design
4 Module IV – Fundamentals of Clinical Trial Conduct & Monitoring
5 Module V – Essential Documents in Clinical Trials
6 Module VI – Medical Devices regulations & GMP basics
7 Module VII - Networking, Job search, Interview preparation
CRC Certification Program: Basics of ICH GCP
1 Module I – Introduction to Clinical Research *
2 Module II – Essentials of ICH GCP & FDA regulations
3 Module III – Basics of Clinical Trials Design
4 Module IV – Fundamentals of Clinical Trial Conduct
5 Module V – Essential Documents in Clinical Trials
6 Module VII - Networking, Job search, Interview preparation
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* Module I is a prerequisite for Module II as it contains essential information | 
