still-life-business-roles-with-various-mechanism-pieces

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

clinical-trials-overview

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.