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 project management
 clinical monitoring
 safety -    pharmacovigilence
 data management
 market research
 medical writing
 medical/scientific    translations
 clinical quality assurance

e-CRF creation through collaboration with external specialists
Database set-up and creation of an annotated CRF Safety review of incoming CRFs
Single data entry, data validation checks, run validation programs
  and generation of DCFs
SAE reconciliation in close collaboration with the Sponsor