Competence in therapeutic niches Sprache wechseln zu Deutsch
For us "quality, time and costs"
are the most important criteria in clinical research
We offer
quality assurance in clinical research of drugs and other medical products (clinical trials and post marketing surveillances)
  • Coordinating and conducting clinical trials in phase II to phase IV and post marketing surveillances in accordance with national and international standards, laws and regulations
  • Writing of study protocols and case report forms
  • Submission of study protocols to the IRB/IEC
  • Applications to the competent authorities, Federal Office for Radiation Protection and notifications to the local authorities
  • Coordinating and conducting investigator meetings
  • Monitoring
  • Statistical analyses of study data in cooperation with established biometric institutes
  • Writing of final study reports
  • Investigator training and qualification of study personnel
  • Writing of Standard Operating Procedures (SOPs)
  • GCP audits
Clinical Trials