Clinical Operations group executes Clinical Trials in Phases I-IV for leading Pharmaceutical and Biotech Companies, preserving the supreme standards of ethics, confidentiality and quality. Our well-trained team has a combined experience in project management in several therapeutic areas.
We promote a team approach with Accentuate on support, personal development, training, management, accountability, and recognition. To assure
our clients receive quality monitoring services in assent with the applicable Regulatory guidelines, we provide complete Developmental and training program to our Clinical Research Associates (CRAs), Clinical Research Coordinator (CRCs) and Project team members.
Clinical Operation includes:
- Clinical Protocol Development
- Regulatory Processes
- Clinical Site Selection, Training and Management
- Clinical Monitoring
- Safety Monitoring
- Data management
- Statistical Analysis of Clinical Data
- Human Subject Protection and Ethics
