We provide our clients with uncompromised, customised service on clinical studies ranging from initial strategic planning through regulatory submission and approval.

Clinical Research:
  • Pre-Study activities with organisation of investigators meetings
  • Site selection /Pre-study qualification
  • IRB application/submission preparation
  • Study recruitment
  • Project Management/Clinical Trial Management
  • Monitoring – Site initiation, Interim, Close-out
  • Data Management and Biostatistics Services
  • Regulatory documentation
Medical Writing:
  • Protocol development and writing
  • Informed Consent writing
  • Investigator's brochures
  • Case Report Form design
  • Operation manuals
  • Report writing
  • SOP writing
  • Medical – abstracts, manuscripts, posters, patient info leaflets, drug monographs
  • Clinical study reports – integrated summaries, study summary reports, non-clinical study reports, expert reports
  • Marketing and training materials
  • White papers and new drug applications