Course Topics

  • 1

    How to use the platform.

    • Introduction

    • How to Communicate to Answer Your Questions

    • How to navigate the course options.

    • Appreciation

    • Course Planner

    • Fair Reminder - Please Pay Attention

  • 2

    I. Basics

    • Chapter 1 Lecture 1 - What is Pharmacovigilance & Its History

    • Chapter 1 Lecture 1 - Arabic

    • Chapter 1 Lecture 1 PDF

    • Chapter 1 Lecture 1 Quiz.

    • Chapter 1 Lecture 2- What is Drug Development Process?

    • Chapter 1 Lecture 2 - Arabic

    • Chapter 1 Lecture 2 PDF.

    • Chapter 1 Lecture 2 Quiz.

    • Chapter 1 Lecture 3- Introduction of Reporting Requirements in Pre-Marketing.

    • Chapter 1 Lecture 3 - Arabic

    • Chapter 1 Lecture 3 PDF

    • Chapter 1 Lecture 3 Quiz.

    • Chapter 1 Lecture 4 - Introduction of Reporting Requirements in Post-Marketing.

    • Chapter 1 Lecture 4 - Arabic

    • Chapter 1 Lecture 4

    • Chapter 1 Lecture 4 Quiz.

    • Final Quiz for Chapter 1

  • 3

    II. Pharmacovigilance Terminology

    • Chapter 2 Lecture 1 - Clinical Trials Terminology

    • Chapter 2 lecture 1 - Arabic

    • Chapter 2 Lecture 1 PDF.

    • Chapter 2Lecture 1 Quiz.

    • Chapter 2 Lecture 2 - Adverse Events Terminology

    • Chapter 2 Lecture 2 - Arabic

    • Chapter 2 Lecture 2 PDF.

    • Chapter 2 Lecture 2 Quiz.

    • Chapter 2 Lecture 3 -Data

    • Chapter 2 Lecture 3 - Arabic

    • Chapter 2 Lecture 3 PDF.

    • Chapter 2 Lecture 3 Quiz.

    • Final Quiz for Chapter 2

  • 4

    III. Company Safety Unit Roles & Workflow.

    • Chapter 3 Arabic Lecturs

    • Chapter 3 Lecture 1 - Pharmacovigilance Department

    • Chapter 3 Lecture 1 PDF - B.

    • Chapter 3 Lecture 1 Arabic - Part 1

    • Chapter 3 Lecture 1 Arabic - Part 2

    • Chapter 3 Lecture 1 Quiz.

    • Chapter 3 Lecture 2 - Other roles in the Drug Safety Department.

    • Chapter 3 Lecture 2 - Arabic - Part 1

    • Chapter 3 Lecture 2 Arabic - Part 2

    • Chapter 3 Lecture 2 PDF.

    • Chapter 3 Lecture 2 Quiz.

    • Chapter 3 Lecture 3 - Drug Safety Case Process in Clinical Trials Phase

    • Chapter 3 lecture 3 Arabic

    • Chapter 3 Lecture 3 PDF.

    • Chapter 3 Lecture 3 Quiz.

    • Chapter 3 Lecture 4 - Drug Safety Case Process in Post-Marketing Phase

    • Chapter 3 lecture 4 Arabic

    • Chapter 3 Lecture 4 PDF

    • Chapter 3 Lecture 4 Quiz.

    • Chapter 3 Lecture 5 - Drug Safety Case Process in Post-Marketing Phase - The Third Department

    • Chapter 3 lecture 5 Arabic

    • Chapter 3 Lecture 5 PDF

    • Chapter 3 Lecture 5 Quiz.

    • Chapter 3 Lecture 6 - MedDRA Coding & Dictionary Maintenance

    • Chapter 3 lecture 6 Arabic

    • Chapter 3 Lecture 6 PDF

    • Chapter 3 Lecture 6 Quiz.

    • Final Quiz for Chapter 3

  • 5

    IV. Reference Safety Information

    • Chapter 4 Lecture 1 - Reference Safety Information

    • Chapter 4 Lecture 1 PDF.

    • Final Quiz for Chapter 4

  • 6

    V. Pharmacovigilance Reporting

    • How to Fill Yellow Card

    • Its PDFs

    • How to fill ICSR

    • ICSR Templates

    • +70 Downloadable PDFs Educational Materials about Drug Development & Pharmacovigilance

    • Educational Resources

    • CAPA Template

    • What is PSUR?

  • 7

    VI. Advanced Pharmacovigilance Modules

    • Post-marketing Safety Management

  • 8

    VII. Graduation Projects.

  • 9

    VIII. How to Report Like a Professional - Additional Free Bonus

    • Welcome to Huge additional Bonus

    • Please Follow this Video Steps to Understand the Process

    • CDC VAERS

    • 5 PDFs about Pharmacovigilance

    • 5 PDFs about Pharmacology

    • Links for Educational Resources