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Our clinical studies
We provide high-quality, end-to-end or specific and flexible, clinical trial services across different therapeutic areas, covering from early Phase I to late Phase IV and Real World Evidence studies. We have an experienced team that can work collaboratively to design and customize the solution to the client’s needs. We can support the full study or provide tailored consultancy activities.
Services include:
- Study design and protocol development/writing
- Full epidemiological feasibility study and report
- Clinical project management
- Vendor selection and management, including global logistics management
- Site identification, feasibility and selection
- Start-up, IRB/EC and RA submissions
- Site management and clinical monitoring
- Site capability and capacity building
- Investigator payments
- Medical monitoring
- Patient safety and pharmacovigilance
- Data management
- Biostatistics
- Medical writing and publishing
- Quality and audit management and inspection readiness
Other services
We offer a wide range of projects. Click on the icons below for more info.
Epidemiology and RWE
Primary data collection studies, database studies, and systematic literature reviews
Medical writing
Document writing and editing, conference presentations, meeting reports
Pharmacovigilance
Safety monitoring, signal detection, analysis, regulatory documents, and training
Qualitative Research
Interviews, focus groups, questionnaires, with analysis and reporting
Statistics/IT
Data management, analysis and reporting