Events

Quartica provides services to manage the end to end aggregate reporting process from planning, development and review of deliverables to submission to the health authority. Our team of experts can provide you with the right expertise for the development and submission of the following aggregate reports:

  • FDA Government
  • European Medicines Agency
  • Orphan Drug Designation Annual Report
  • PADER: Periodic Drug Adverse experience Report
  • PSUR: Periodic Safety Update Reports
  • PSUR: Periodic Safety Update Reports
  • SBR: Summary Bridging Report
  • ACO: Addendum to Clinical Overview