Tailored Services For Your Study
Use our solutions for full-study execution or to fill capability gaps. Our offerings include:
Study Design & Protocol Development
Our clinical, operational and biostatistical experts work with you to develop scientifically rigorous, practical protocols aligned with your research objectives and regulatory requirements.
Feasibility
Combining data, local knowledge and established investigator networks, we assess patient access, site readiness and operational considerations to recommend realistic study plans.
Regulatory
Our experienced regional teams support submissions, ethics reviews and ongoing regulatory activities, giving sponsors access to local insight and meeting requirements across multiple jurisdictions.
Rapid Study Start up & Site Activation
We coordinate the activities needed to move sites efficiently from selection through activation, applying experience gained in complex and time sensitive research settings to move your research into the clinic.
Recruitment & Retention
Working with Sponsors, sites and local partners, we develop recruitment and retention approaches that reflect the needs, barriers and context of the populations your study aims to reach.
Site Selection, Management & Training
We use established investigator relationships and global site networks to identify appropriate sites appropriate for your research, then provide tailored training and ongoing support throughout delivery.
Project Management
Dedicated project teams coordinate timelines, budgets, risks and cross functional delivery. We provide each Sponsor with responsive support and access to experienced leadership throughout every study.
Clinical Monitoring
We tailor monitoring to study risks and site conditions, combining onsite, remote and centralized oversight to reach your goals while supporting participant safety, protocol compliance and reliable data.
Medical Monitoring
Experienced physicians provide clinical oversight, review emerging medical issues and support sponsors and investigators throughout the study.
Pharmacovigilance
Our physician-led pharmacovigilance team provides safety surveillance, case assessment and regulatory reporting, integrated closely with medical monitoring and the wider study team.
Data Management & Biostatistics
Our specialists provide integrated data management and biostatistical support from study design through database close and final analysis, with systems tailored to your programme’s needs.
Medical Writing
Our medical writers work closely with Sponsors and with clinical and statistical teams to develop clear, scientifically accurate reports and technical documents aligned with study and regulatory requirements.
Laboratory Support
We help Sponsors identify qualified laboratory services, and align laboratory requirements with site capabilities, then coordinate laboratory activities to support consistent processes and dependable study data.
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.
