We specialise in the planning, execution, analysis, reporting and management of phase II-IV clinical trials across different therapeutic areas. We have access to a network of multi disciplinary investigators and leverage on their extensive clinical trial experience and expertise in the public, private and university hospitals in order to achieve your clinical trial objectives
Our comprehensive solutions and customised services to simplify your journey to market:
- Feasibility Studies
- Protocol Design and Development
- Site & Investigator Identification
- Contract & Study Budget Negotiation
- Study Initiation
- IRB/ IEC Ethics Application
- Regulatory Affairs
- CTIL/CTX Application
- Clinical Trial Monitoring
- Clinical Trial Logistics
- Safety Surveillance
- Site Management
- Data Management & Biostatistical Analysis
- Study Close Out
- Final Study Report
- Records Retention Management
- Project Management
