Pharmacovigilance Training & Services

Veeda’s one stop Pharmacovigilance solutions offer a broad spectrum, high quality, flexible, cost effective and scalable safety monitoring services, that can fit seamlessly into your process, meeting all regulatory compliance requirements.

We provide a global strategy for a cooperative partnership with our clients in drug safety management for US, EU and ROW countries.

The team is powered by highly specialized pharmacy and medical professionals. We endeavors to constantly build on optimal processes complimenting your needs

  • Preparation of Pharmacovigilance System Master File
  • Qualified Person for Pharmacovigilance (QPPV) and Local Responsible Person for Pharmacovigilance (LRPV)
  • Individual Case Safety Report (ICSR) Processing of Initial/Follow-up reports – including medical review
  • Global Expedited Case Reporting
  • Literature screening
  • Aggregate report writing – PSUR, PBRER, PADER and ACOS
  • Risk Management Plan production and review
  • Signal Detection and Evaluation
  • Pharmacovigilance Consultancy and Training
  • Recommendations for Pharmacovigilance department designing, development and improvement.
  • Pharmacovigilance Quality Assurance including SOP development
  • Audits and support for Inspections
  • Extended EudraVigilance Medicinal Product Dictionary (XEVMPD) entries and maintenance