• Trial concept design and medical writing (study protocol to final report)
  • Monitoring of clinical trials (Phase I-IV in all indications)
  • Conduct of early phase trials (in patients or healthy volunteers) in our own University Hospital-based Clinical Research Unit for Phase I, BA/BE Studies
  • Site management
  • Biostatistics, data management, web-based clinical trial management systems (CTMS), EDC
  • Development and validation of bioanalytical assays using HPLC and LC-MS/MS
  • Independent external QA audits and co-monitoring
  • GCP and regulatory training for investigators and health care professionals
  • Regulatory consultancy
  • Quality of Life Projects: translation, pilot testing, proofreading and validation
  • Epidemiological and Pharmaceutical Market Research