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European Experts for Clinical Research

e&e cro consulting

Design, Planning and Execution of multicentre trials to current GCP and ICH EN ISO 14155 guidelines since 1991.

COMPLETE PROJECT ORGANISATION

  • Advice in Investigational Site Identification
  • Preparation of Study specific documents
  • National Competence Authorities and Ethic Committees’ Submissions
  • Site & Data Management
  • SAE reporting, Amendments, Notifications, Review
  • Case Support
  • Study Material Logistics & Device Accountability
  • On-site Monitoring and Reporting

Our domains – One solution

Cardiovascular

Cerebrovascular

Emergency medicine

oncology diagnostics