CRAs working independently provide clinical trial services and consulting trough Phase I - IV clinical trials for local and international pharmaceutical, biotech companies and contract research organizations. Activities provided are strongly based on ICH/GCP guidelines, EU directives and local legislation.


Partners: Poland, Croatia, Hungary, Czech Republic, Russia and Ukraine.


Areas of expertise: Cardiovascular diseases, Oncology, Pulmonary diseases, CNS and Psychiatric disorders, Endocrine and Metabolic diseases, Infectious diseases and Medical devices.


Services:

  • Feasibility assessments
  • Protocol review
  • CRF design
  • Investigator recruitment
  • Site and investigator selection
  • Regulatory and Ethics Committee approvals
  • Investigator Meeting organization
  • Site management (training, initiation, monitoring, AE reporting and close-out)

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