Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 8-9 September 2025 Riyadh Saudi Arabia

Venue

Details

Overview

FEES

SAUDI RIYAL

REGISTRATION FEES

SAR 6500.00

EARLY BIRDS REGISTRATION FEE

PAY YOUR FEE BEFORE 6 September 2025.

SAR 5200.00

OVERVIEW

Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

Download Brochure Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate_8-9 September_2025 Riyadh

Note This training program requires physical presence and will be held in Riyadh at Bawazir Pharma Center

Learning Objectives

At the conclusion of this training, participants will be able to:

Define the key principles and processes of pharmacovigilance

Define official regulatory policies and other issues pertinent to SFDA Pharmacovigilance System
Describe the component of the PV System
Understand the role and responsibilities of the QPPV
Understand national pharmacovigilance sub-system file (national PSSF)
Recognize SFDA oversight and processes during the post-approval phase.
Understand ADR case assessment, PSUR and risk management.
Interact appropriately with the SFDA regarding PV
Understand the process of PV inspection and audits.