Clinical Science

DNA graphic, Medical Affairs page
  • Development and thorough execution of study Medical Review Plans
  • Medical assessment of Serious Adverse Events (SAEs)
  • In depth scientific review of study related documentation and procedures, including electronic Case Report Forms (CRFs), Data Management Checks, Statistical Analysis Plans (SAPs), Clinical Monitoring Plans
  • Study Proposals development
  • Protocols development
  • Informed Consent Forms (ICFs) development
  • Clinical Study Reports (CSRs) development
  • Manuscripts development
  • Authoring of posters and abstracts
  • Development of interactive training courses across a range of diseases in hemato-oncology
  • Development of rigorous assessments to ensure true understanding of assigned protocols and related therapeutic areas

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