 |
Selection of site/Investigator
of any therapeutic areas |
|
Protocol Development |
|
CRF Designing |
|
Co-ordination of Ethics
Committee Approval |
|
Site Monitoring |
|
Site Initiation Activities |
|
Clinical Trial Management |
|
Data Management and statistical
Analysis |
|
Clinical Report Preparation |
|
Training |
|
Archiving |
|
Preparation & Submission
of Regulatory Documents |
