Our CRO services
Study preparation, site management and clinical monitoring, with services tailored to the needs of your study.
Discuss your studyStudy coordination from protocol preparation through site close-out.
View service- Protocol development and site feasibility
- Ethics committee and regulatory submissions
- Study start-up and clinical monitoring
- Data management
Sourcing, distribution and tracking of study equipment and materials.
View service- Equipment and supply planning
- Logistics, distribution and inventory tracking
- Device records and regulatory compliance
- Recall and waste management
Management of study timelines, budgets and workflows across teams.
View service- Project plans and timelines
- Budget, resource and risk tracking
- Site, sponsor and vendor coordination
- Quality oversight, reporting and close-out
Studies evaluating product safety and effectiveness after approval.
View service- Phase IV and observational studies
- Long-term safety and effectiveness follow-up
- Pharmacovigilance and regulatory reporting
- Collection of real-world usage data
Analysis of routine healthcare data to address a defined research question.
View service- Study design and protocol development
- Data collection, integration and statistical analysis
- Safety and comparative effectiveness research
- Health economics and outcomes research (HEOR)
Analyses of the economic value and market access of healthcare products.
View service- Health economic analyses
- Market access and reimbursement planning
- Value proposition development
- Health technology assessment (HTA)