Project Log

Qmed´s excellent track record is reflected in our good reputation in the industry, with 100% of our business coming from existing client referrals.

  • Medical writing (CIP, IB, Reports and articles) – 24 trials
  • Clinical monitoring – 110 trials
  • Biostatistics and datamanagement – 20 trials
  • CPM or CRA management – 28 trial
  • Safety management – 12 trials
  • Submission to EC/IRB or authorities (incl FDA, CAD, AUS) – 96 submissions
  • Strategic consulting – 22 trials
  • Quality projects - 35
  • Regulatory – 157 projects
  • 510(k) – 7 submissions
  • Clinical and biological literature evaluation – 63
  • STED documentation and statement of conformity – 74
  • Regulatory strategy – 25
  • Risk Management – 15
  • Submission – 27
  • Training sessions - 30