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 Service
- RA Core team located in the EU
- Local RA team established in every EMEA country where we operate
Integrated Services
- Pharmacovigilance (located in the EU)
- 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.