Well experienced country-based ( Mexico) pharmacovigilance expert who can support in person to takecare of ther following activities locally.

  • Pre-market Approval
  • Adverse Events Reporting for Bio study and registered products
  • Pre-market Approval
  • Preparation of Marbetes, IPPsPPs
  • Online platform to file Adverse event (R2, R3 XML output)
  • Monitoring and tracking the AE data.

Also, we have Expert committee by the freelance consultant group who supports and provide guidance related to Pharmacovigilance activities which include a group of Doctorate in Pharmacology and clinical and Doctors.