Qaulconform

How We Can Help With POST-MARKET SURVEILLANCE & COMPLIANCE

  • Medical Device Reporting (MDR) system implementation

  • Post-market surveillance planning

  • Recall strategy and management

  • Complaint handling systems

  • Pharmacovigilance system design and implementation

  • Periodic safety update report (PSUR) preparation

  • Risk evaluation and mitigation strategy (REMS) development

  • Product quality complaint handling

  • Serious adverse event reporting system

  • Post-market surveillance for dietary supplements

  • Product recall procedures and mock recalls

  • Customer complaint handling and trending

  • Reportable Food Registry compliance

  • Food safety recall procedures and simulations

  • Foodborne illness investigation support

  • Consumer complaint tracking and analysis

  • Adverse event reporting system for cosmetics

  • Cosmetovigilance program development

  • Product withdrawal and recall procedures

  • Customer feedback analysis for safety signals

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