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TWB PPT - Program Outline

Introduction: Clinical Trial Domain Overview<br>Key Topics:<br>Concepts in Clinical Pharmacology<br>Global Pharmacovigilance Regulations (USA, Europe, India, etc.)<br>Medical Coding and Literature Search<br>Case Assessment and Processing<br>Safety Narrative Writing and Aggregate Reporting<br>Signal Detection and Risk Management<br>

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TWB PPT - Program Outline

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  1. Introduction to PV-Pro Pharmacovigilance Training and Internship

  2. What is Pharmacovigilance? • Definition: The science dedicated to detecting, assessing, and preventing adverse effects of drugs. • Scope: Encompasses drug safety from R&D through post-marketing surveillance. • Importance: Crucial for regulatory authorities, pharmaceutical companies, and healthcare providers.

  3. Program Outline • Introduction: Clinical Trial Domain Overview • Key Topics: • Concepts in Clinical Pharmacology • Global Pharmacovigilance Regulations (USA, Europe, India, etc.) • Medical Coding and Literature Search • Case Assessment and Processing • Safety Narrative Writing and Aggregate Reporting • Signal Detection and Risk Management

  4. Course Features • Comprehensive Training: End-to-end theoretical & practical pharmacovigilance training. • Real-World Application: Simulated projects using the Clinevo Safety Database. • Industry Exposure: Regular assessments and internships for practical experience. • Support: Access to course materials, doubts resolution, and mentorship.

  5. Placement Assistance and Career Support • Internship: Gain hands-on experience as a project intern with The Whiteboard. • Placement Assistance: Expert guidance to secure job placements in the industry. • Certification: Receive an industry-recognized course completion certificate and experience letter.

  6. Contact Information • For More Details on Pharmacovigilance Training: • Phone: 9160794975 • Email: info@thewhiteboard.co.in • Website:The Whiteboard Get Certified, Get Ahead: Transform Your Professional Path with PV-Pro’s Pharmacovigilance Program!

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