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Clinical trials
deutsche Version

Our service in the context of clinical trials

  • Extensive consulting and selection of the adequate study design
  • Planning and preparing of the trial protocoll
  • Preparing of study documentation such as CRF, patient brochures and investigator maunals
  • Administration and preparation such as investigator recruitment, requests to Ethic Committees, notifications to Health Authorities
  • Organisation and conduct of investigator meetings  
  • Monitoring: Initiation of trial centres, On-site-Monitoring, monitoring by phone- and computer
  • Budget management
  • Progress status reports
  • Data management including data base development, query management, medical coding, AE and SAE processing
  • Statistical analysis and integrated study report
  • Preparing of scrips for publications

An optimized study design saves time and money!


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