Pharmacovigilance

Safety monitoring of medicinal products
Safety monitoring
Data security
21 CFR Part 11 compliance
User-friendly interface
Quick-responding tech support

Timely informing about side effects and report generation

  • Unified data collection format
  • Data coding according to MedDRA and WHO Drug
  • Risked factors detection
  • Reporting compliant with regulatory standards
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Other solutions

MATRIX CTMS  —
Complex control of clinical trial
MATRIX IWRS —
Trial subjects randomization
Trial supply —
Planning and dispensing of drugs