Pharmacovigilance Training

Pharmacovigilance training — case processing, MedDRA coding, signal detection basics, ICSR handling, and regulatory reporting timelines.

What is Pharmacovigilance Training?

This programme builds working pharmacovigilance (PV) competence. You learn how adverse event reports flow through a PV system, how cases are coded and narrated, and what regulators expect at every reporting milestone.

What you will learn

PV concepts — ADR vs AE, seriousness, expectedness, causality
ICSR (Individual Case Safety Report) structure and lifecycle
MedDRA coding — hierarchies, LLT/PT selection, coding conventions
Narrative writing — clear, factual, audit-ready
Reporting timelines — CDSCO, FDA, EMA expedited and periodic reports
Signal detection basics — disproportionality concepts, PSUR overview

Who this is for

Freshers from pharmacy, life sciences, biotechnology, and medicine aiming at PV associate, case processor, or drug-safety roles. Equally suited to working professionals moving into a regulated PV team.

What you take away

NTHRYS training certificate detailing PV scope
A capstone case-processing portfolio (mock ICSRs end-to-end)
MedDRA coding and narrative-writing fluency
A direct profile for PV / drug safety roles in pharma and CROs

Pick the field below to see specific PV training options.

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