End to end solutions for research and development projects

Solutions for Research & Development

We are committed to providing comprehensive support throughout the entirety of your research and development project.

Pre-Clinical

  • Medical Writing
  • Regulatory Affairs
  • Translation
  • Vigilance
  • Central Labs
  • GMP Consulting
  • ISO Certifications (specific for Medical Devices)

Phase I-III Clinical Development

  • Regulatory Affairs
  • Clinical Operations
  • Safety Monitoring
  • Medical Writing
  • Vigilance
  • Translation
  • Third Party Audit
  • GMP Consulting
  • Bioanalysis
  • Supply Chain
  • Central Labs
  • Recruitment
  • Site operations

Laboratories in Europe, US, and China

Quality, Scientific Integrity, Regulatory Compliance

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Integrated Platform.
Tailored Solutions.

We incorporate scientific excellence and product development strategy with expertise in early phase clinical research, pharmacology, PK/PD modeling & simulation, and the full range of supporting services.

MAA (NDA & BLA),
Registration

  • Vigilance
  • Regulatory Writing
  • Registration
  • Translation

Post Market / RWS

  • Post-market Research
  • Real World Study
  • Investigator-Initiated
  • Trial
  • Safety Monitoring
  • Medical Affairs
  • Translation
  • Vigilance
  • Market Access
  • Reimbursement
  • Post Registration Activities

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.
Contact us now!