The company, originally founded in 2000, draws on more than 20 years of expertise in the healthcare sector and is based in Czech Republic.

Pharma

Medical Devices​

Combined Services​

  • Clinical Research Organisation – Pharmaceutical
  • Pharmacovigilance consultancy
  • QP PV responsibility
  • Market Access Consultancy
  • Training GCP
  • Clinical Research Organisation – Medical Device and In-vitro-Diagnostics
  • Vigilance support
  • Person Responsible for Regulatory
  • Compliance (PRRC) acc. §15 MDR
  • Training MDR and CER
  • Biomedical development
  • Regulatory Affairs support
  • Quality Assurance
  • European Authorized Representative
  • Medical Writing of regulatory documents
  • Audit and Inspections
    providing Interim Manegement

One step ahead.​

More than 20 years in medical research.​