S.
# |
Course
Titles |
Course
Duration (days) |
1. |
The Indian
Regulations of Clinical Research |
2 |
2. |
Know what
Schedule Y states! |
2 |
3. |
Regulatory
Dossier Compilations for Clinical Trial Approval Submissions |
2 |
4. |
The ICH
- GCP Guidelines |
10 |
5. |
Bioavailability
/ Bioequivalence Guidelines |
1 |
6. |
Advanced
Course in Clinical Research Methodologies |
3 |
7. |
Protocol
Writing |
1 |
8. |
Protocol
Writing & Case Report Form Designing |
3 |
9. |
Informed
Consent Documentation Process |
1 |
10. |
All you
need to know about Drug Safety Management –
Pharmacovigilance; as a Clinical Research personnel |
1 |
11. |
Guidelines
to become the Empowered CRA in the Clinical Research Industry |
2 |
12. |
The tools
to use and move on the fast-track in the Clinical Research Industry |
2 |
13. |
How to
become the favourite Study Coordinator of all the Monitors? |
3 |
14. |
The secrets
of effective Monitoring in Clinical Research |
2 |
15. |
Precise
Communication Skills of Clinical Research Personnel |
2 |
16 |
The insights
of a successful Ethics Committee in Clinical Research |
3 |
17. |
Quality
Assurance vs. Quality Control in Clinical Research |
5 |
18. |
How to
groom yourself into a Clinical Research Auditor? |
5 |
19. |
Designing Standard
Operating Procedures in Clinical Research |
3 |
20. |
Guidelines
for Effective Documentation practices in Clinical Research |
2 |
21. |
Guidelines
to become a Clinical Research Investigator |
5 |
22. |
What is
Project Management in Clinical Research? |
2 |
23. |
Post-Marketing
Surveillance study details |
1 |
24. |
Conducting
Clinical Studies using Medical Devices |
1 |
25. |
Data Management
in Clinical Research |
3 |
26. |
Biostatistics |
2 |
27. |
Personality
Grooming of Self |
1 |