Once this course completed, You are eligible to get certificates as
Advanced PG Diploma in Clinical Research
| Module 1 | Clinical Research | |
|---|---|---|
| Unit 1 | 1. Introduction to Clinical Research & Good Clinical Practice | |
| Unit 2 | 2- Overview ICH GCP | |
| Unit 3 | 3. Good Clinical practice | |
| Unit 4 | 4. Clinical Trails | |
| Unit 5 | 5. Institutional Reviews board | |
| Unit 6 | 5. Institutional Reviews board | |
| Unit 7 | 6. Investigation Responsibilities in clinical trails | |
| Unit 8 | 7. Roles and Responsibilities of Sponsor & Clinical Trial Monitor | |
| Unit 9 | 8. Informed Consent Process | |
| Unit 10 | 9. Serious Adverse Event (SAE), Adverse event reporting | |
| Unit 11 | 10. Site Initiation visit | |
| Unit 12 | 11. Site close visit | |
| Unit 13 | Test Your Self | |
| Unit 14 | Apply Your Certificate |
