Contents:
1. Clinical
Research – A Clinical Investigator’s Perspective
2. Medical
Device Development, Process and Regulation
3. Preclinical
Drug Development
4. Phases
of Clinical Trials
5. Phase
0 – Micro dosing Studies
6. Clinical
Research Planning
7. Clinical
Research Design
8. Clinical
Research Protocol
9. Designing
Case Report Forms
10. Process
of Randomization in Clinical Trials
11. Investigational
Medicinal Products
12. Multi
center Clinical Trials
13. Good
Clinical Research Practice
14. Role
and Responsibilities of Sponsor
15. Role
and Responsibilities of Principal Investigator
16. Ethical
Consideration in Clinical Research – Special Reference to Developing
Countries
17. Informed
Consent in Clinical Research
18. Monitoring
in Clinical Trials
19. Quality
Assurance in Clinical Research
20. Pharmacovigilance
and Drug Safety
21. Data
and Safety Monitoring Board and Monitoring Plan
22. Standard
Operating Procedures
23. Archiving
Clinical Research Documents
24. Evidence
Based Medicine
25. Clinical
Research Data Management
26. Clinical
Biostatistics, (a) Biostatistics for clinical Researcher, (b)
Terminology used in Biostatistics |