Skill Development Programme on Pharmacovigilance Organized by the Indian Pharmacopoeia Commission (IPC), Ministry of Health & Family Welfare, Government of India
Mode: Online | Duration: 18th – 22nd August 2025
Registration Deadline: 12th August 2025 | Fee: ₹2000
🏛️ About the Programme:
The Indian Pharmacopoeia Commission (IPC), functioning as the National Coordination Centre (NCC) for the Pharmacovigilance Programme of India (PvPI) and a WHO Collaborating Centre, is pleased to announce the 34th edition of its highly reputed Skill Development Programme on Pharmacovigilance. This online training course is designed to equip participants with comprehensive knowledge, applied skills, and the regulatory understanding necessary for excellence in the field of pharmacovigilance and drug safety monitoring.
With the rising significance of adverse drug reaction (ADR) reporting, drug regulation, and post-marketing surveillance, pharmacovigilance is now a cornerstone of public health and pharmaceutical care. This programme stands as a critical platform for capacity building and continuous professional development in pharmacovigilance and regulatory science.
🎯 Programme Objectives:
- To create awareness about the importance of pharmacovigilance in ensuring patient safety.
- To train healthcare professionals and students on the tools and techniques of ADR monitoring and reporting.
- To explain national and international regulatory frameworks governing pharmacovigilance.
- To develop expertise in risk-benefit evaluation, signal detection, and safety communication.
- To strengthen institutional and individual capacity for contributing to India’s pharmacovigilance ecosystem.
👩⚕️ Who Should Apply?
The programme is ideal for students, early-career professionals, and seasoned experts from the following backgrounds:
- Pharmacy (B.Pharm, M.Pharm, Pharm D)
- MBBS and BDS graduates or students
- Nursing professionals and nursing students
- Practicing Pharmacists, Doctors, and Nurses
- Academicians and faculty members from health sciences
- Industry professionals involved in drug safety, regulatory affairs, clinical research, or QA/QC
Note: Individuals representing NGOs or consumers are currently not eligible for this specific training.
📚 What You Will Learn:
The training content is meticulously curated by experts from IPC and PvPI, covering topics including:
- Introduction to Pharmacovigilance and Drug Safety
- Indian Regulatory Landscape: Role of IPC, CDSCO, and PvPI
- Global Pharmacovigilance Practices: WHO and UMC Guidelines
- Spontaneous ADR Reporting and Data Collection Tools
- Signal Detection and Risk Management
- Causality Assessment and Case Studies
- E2B Reporting Standards and Software Tools
- Ethical Aspects and Legal Implications of Drug Safety Monitoring
- Safety Communication and Patient Engagement
🧾 Programme Details:
- 🗓️ Dates: 18th – 22nd August 2025
- 🖥️ Mode: Online (accessible nationwide)
- 💳 Registration Fee: ₹2000 (non-refundable)
- ⌛ Last Date to Register: 12th August 2025
- 📜 Certification: Participants will receive an official certificate only after successfully completing:
- Pre-assessment
- Post-assessment
- Feedback form submission
📝 Registration Process:
- Step 1: Scan the QR code to make the payment of ₹2000.
- Step 2: Scan the second QR code to complete your registration by filling out the required details.
Online Payment Link: Click here
Online registration link: Click here
Ensure that both steps are completed before the registration deadline. Late or incomplete submissions will not be entertained.
📞 Contact Information:
If you need any assistance regarding registration, payment, or participation, feel free to reach out:
- 📧 Email: [email protected]
- ☎️ Phone: 0120-2783400 Ext. 145
- 🌐 Website: www.ipc.gov.in
📌 Why You Should Attend:
In an era where drug safety has become a public health priority, pharmacovigilance training is not just a qualification — it’s a necessity. Whether you’re a student exploring your career path or a professional aiming to stay updated with regulatory science, this programme will empower you to:
- Contribute to patient safety and rational use of medicines.
- Participate in national pharmacovigilance initiatives.
- Understand regulatory documentation and risk assessment.
- Strengthen your CV with a government-recognized certification.
- Network with experts and peers in the field of healthcare and pharmaceutical sciences.
💡 About IPC and PvPI:
The Indian Pharmacopoeia Commission (IPC) is an autonomous institution under the Ministry of Health & Family Welfare, Government of India. It is entrusted with setting standards for drugs and driving regulatory harmonization across India. IPC also serves as the National Coordination Centre for the Pharmacovigilance Programme of India (PvPI), aimed at ensuring medicine safety through ADR monitoring and post-marketing surveillance.
As a WHO Collaborating Centre, IPC also works closely with global partners to align India’s pharmacovigilance ecosystem with international best practices.
🔍 Join the 34th Skill Development Programme on Pharmacovigilance and become a certified contributor to India’s healthcare and drug safety system.
🕒 Seats are limited. Register today and secure your place!