Full Suite of Capabilities
Integrated Platform with End-to-End Service Offerings
Clinical Operations
- Drugs
ADCs, CART, Ab, small molecules... - Medical Device & IVD
- Vaccine
- Nutraceuticals & Cosmetics
- Feasibility
- EC & CA submission
- Clinical Project Management
- Clinical Trial Monitoring
- Site Management
- Subject Recruitment
Biometrics
- CRF/e-CRF Development
- Data Management
- Statistical Analysis
- Study Drug Allocation
Regulatory Affairs
CTR and MDR Submission and Consulting ServiceRA Core team located in the EU
Local RA team established in every EMEA country where we operate
Integrated Services
Medical Monitoring (located in the EU)
Medical Writing
Legal Related Areas of Expertise
Clinical research
Pharma law
Business law
Contract law
Data Protection
Intellectual property
Anti-bribery and Corruption
Corporate Governance and Compliance
Tax law
Labor law
Real estate
Dispute resolution
Partner with us to reach your pharmaceutical objectives
Contact us to develop a tailored clinical trial solution. Our team will guide you from protocol design to patient recruitment, ensuring compliance and optimizing outcomes.