Services
- Site Initiation Visit
- Clinical Trial Monitoring
- Management of Serious Adverse Event Reporting
- Investigational Product Management and Accountability
- Coordination for the Data Management Activities
- Prevention, Management and Escalation of Deviations
- Achieving the Enrolment and Data Management Matrices
- Study Close-out Monitoring Visit
Therapeutic Area Expertise
We have hands-on experience of working on various phase II, III and IV clinical trials in the therapeutic areas of:
- Oncology
- Endocrinology
- Critical Care
- Cardiology
- Andrology
- CNS
- Ophthalmology
- Infectious Diseases
- Medical Devices
- Molecular Diagnostics
- DTx