Clinical Trials
Explore our Clinical Trials Capabilities:
We assist our clients in bringing new and innovative medicinal products to market in a timely and cost-effective manner.
Our expert team works closely with sponsors to tailor the best solution for each project and to deliver clinical trials to the highest quality.
Our highly experienced, locally-based teams allow us to deliver flexible and innovative solutions to accessing patient populations, and ensure that our clinical trials make an impact for sponsors, clinicians and patients
We are proud to provide the following services:
1. Early Phase Clinical trial
Our deep expertise in Phase I research includes studies for:
- First in human
- Human absorption, metabolism, and excretion (AME)
- Healthy normal volunteers
2. Phase 2-3 clinical trials
Our Clinical services include:
- Site identification and selection
- Site contracting and budget negotiation
- Essential documents collection and processing
- Site initiation, interim monitoring, and study closure visits
- Risk-based monitoring
- Overall site management and communication
- Site training and audit support
3. Phase 4 / Post Marketing
We provide the following late phase and post-marketing services:
- Observational studies
- Registry studies (patient, disease, drug and device)
- Phase IV studies
- Retrospective data collection
- Risk-based monitoring
- Post-marketing safety surveillance
Clinical Trials Expertise:
- Regulatory Affairs Consultancy
- Clinical Monitoring and Operations
- Medical Writing
- Study Feasibility
- Data management
- Staff Outsourcing
- Project Management
- Biostatistics
- Site Recommendations