Pharmacovigilance for Drug Safety & Efficacy

Introduction to the Course

Course Objectives

• Understand the basics of pharmacovigilance and its applications in drug safety and efficacy.
• Learn about the detection, classification, and reporting of adverse drug reactions (ADRs).
• Acquire hands-on experience of pharmacovigilance regulations and compliance around the world.
• Become proficient in safety data collection, signal detection, and benefit-risk assessment.
• Delve into post-marketing surveillance and real-world evidence in drug safety monitoring.
• Acquire skills to interpret drug safety data and inform regulatory decisions.

What Will You Learn (Modules)

Module 1 — Pharmacovigilance Basics & Roles

• Explore the foundations of pharmacovigilance, its importance in drug development, and how safety systems are structured.

Module 2 — Adverse Event Reporting & Signal Detection

• Learn methods to identify, document, and manage adverse events, along with tools used for signal detection and trend analysis.

Module 3 — Regulatory Standards & Safety Decision‑Making

• Understand global regulatory frameworks, benefit‑risk assessment strategies, and how to interpret safety evidence for decision‑making.

Who Should Take This Course?

This course is ideal for:

• Pharmacy, life science, and medical graduates aiming for pharmacovigilance careers
• Clinical research professionals and CRO staff
• Pharmaceutical and biotech professionals in drug safety or regulatory roles
• Healthcare professionals involved in ADR reporting

Job Opportunities

After completing this course, learners can pursue roles such as:

• Pharmacovigilance Associate / Officer
• Drug Safety Scientist
• Clinical Safety Specialist
• Regulatory Affairs – Pharmacovigilance

Why Learn With Nanoschool?

At NanoSchool, we focus on career-relevant learning that builds real capability—not just theory.

• Expert-led training: Learn from instructors with real-world experience in applying skills to industry and research problems.
• Practical & hands-on approach: Build skills through guided activities, templates, and task-based learning you can apply immediately.
• Industry-aligned curriculum: Course content is designed around current tools, workflows, and expectations from employers.
• Portfolio-ready outcomes: Create outputs you can showcase in interviews, academic profiles, proposals, or real work.
• Learner support: Get structured guidance, clear learning paths, and support to stay consistent and finish strong.

Key outcomes of the course

Upon completion, learners will be able to:

• In-depth knowledge of pharmacovigilance systems and drug safety lifecycle
• Skill to identify, evaluate, and report adverse drug reactions
• Practical knowledge of global regulatory requirements
• Confidence in post-marketing surveillance and safety data evaluation
• Readiness to enter the job market for pharmacovigilance and drug safety positions