Inspection Readiness in Pharmacovigilance

Inspection Readiness in Pharmacovigilance

📅 Date11 June 2026
🕓 Duration30 minutes

Overview

Pharmacovigilance inspections are becoming more frequent and more rigorous. For CROs and life sciences companies, being inspection-ready is critical to maintaining compliance and credibility.

Join us for an exclusive webinar on “Inspection Readiness in Pharmacovigilance,” scheduled for 11th June 2026. This webinar provides a practical overview of PV inspection readiness, covering key processes, documentation, and training requirements.

Agenda

Points of discussion

Eight focused segments designed to leave you with a working inspection-readiness plan.

01

PV system overview in the context of inspections

02

Importance of inspections for CROs

03

Who conducts PV inspections

04

Types and stages of inspections

05

Training requirements for teams

06

Document management essentials

07

Role of mock inspections

08

Live Q&A with an industry expert

Speaker

Meet the expert

Vijayalakshmi B

ICSR Operations · Senior Subject Matter Expert

Senior subject matter expert in ICSR operations with deep experience supporting global pharmacovigilance inspections, mock audits, and regulatory readiness programs across CROs and sponsors.

Strengthen your Pharmacovigilance Inspection Readiness

Asia-Pacific & Middle East

11:30 AM IST

Register Now →

Europe & Americas

10:00 AM CDT  ·  4:00 PM BST

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