Tailored Services For Your Study
Use our solutions for full-study execution or to fill capability gaps. Our offerings include:
Site Selection & Development
- Feasibility assessments leveraging a vast database of high-quality sites
- Rapid site identification through an established global network
- Industry-standard site feasibility assessments
- Case Study: Conducted 38 site feasibility assessments across 18 countries in two months
Site Management & Training
- Deployment of qualified health response personnel
- Full-time site support for research-naïve staff
- Pre-deployment and protocol-specific training
- Continuous training through online and in-person sessions
- Data management and informed consent training
Project Management
- Site development plans and staff mentoring
- Risk assessment and mitigation strategies
- Defined timelines and deliverables
- Financial oversight to international standards
- Experience: 16-years average staff experience, operations in 70+ countries
Clinical Monitoring
- Study-specific monitoring plans
- Custom recruitment and retention strategies
- On-site and remote monitoring for compliance and risk management
- Clinical Monitors with world class training, living and working where your study is placed
Data Management
- Full-service multi-site, multi-country study support
- Site staff readiness assessments
- Clinical quality management plans and SOP development
- Automated data discrepancy checks
- Experience: 25 years in global data management, with staff averaging 14 years of experience
Biostatistics Support
- Protocol reviews and statistical analysis plan development
- Flexible, validated randomization systems
- Expertise: 5 PhD-level, 6 Master’s-level, and 1 Bachelor’s-level statistician with a median of 19 years of experience
Laboratory Support
- Technical assistance, training, and audits
- Regulatory compliance monitoring
- Track Record: 500+ Good Clinical Laboratory Practice (GCLP) audits, training for 1,500+ lab technicians globally
Regulatory Services
- Study registration and compliance with ethics and regulatory requirements
- Regulatory strategy and documentation oversight
Agile, Responsive, and Results-Driven
Our tailored approach ensures:
- Your research meets and exceeds international quality and ethics standards
- High-quality, consistent study data
- Custom quality improvement strategies
We conduct high-quality studies around the world – in developed and developing countries, in challenging environments and resource-limited settings – ensuring your research meets your needs and your clients’ needs. Our therapeutic experience includes infectious and non-communicable indications, from first-in-human clinical trials through post-marketing surveillance.
