The AQbD Webinar 2026 organized by UPHAR Foundation, Odisha is a free national-level educational webinar designed for pharmacy students, researchers, academicians, and pharmaceutical professionals. The session, titled “Analytical Quality by Design (AQbD): Integration to ICH Guidelines”, will be delivered by Dr. Bikash Ranjan Jena, Associate Professor, Department of Pharmaceutical Analysis, The Neotia University, West Bengal.
This webinar will help participants understand how Analytical Quality by Design (AQbD) integrates with ICH Guidelines to develop robust, reliable, and regulatory-compliant analytical methods for modern pharmaceutical products.
Quick Summary
The AQbD Webinar 2026 is a free 60-minute online webinar organized by UPHAR Foundation, Odisha. Participants will learn the fundamentals of Analytical Quality by Design (AQbD), Design of Experiments (DoE), risk assessment, analytical method development, and integration with ICH Guidelines from an experienced pharmaceutical analysis expert.
AQbD Webinar 2026 Overview
| Particular | Details |
|---|---|
| Webinar Title | Analytical Quality by Design (AQbD): Integration to ICH Guidelines |
| Organizer | UPHAR Foundation, Odisha |
| Speaker | Dr. Bikash Ranjan Jena |
| Designation | Associate Professor, Department of Pharmaceutical Analysis |
| Institution | The Neotia University (Ambuja Neotia Group), West Bengal |
| Date | Sunday, 1 November 2026 |
| Time | 11:30 AM – 12:30 PM (IST) |
| Duration | 60 Minutes |
| Platform | Google Meet |
| Registration | Free |
| Mode | Online Webinar |
Why Is This Webinar Important?
Analytical Quality by Design (AQbD) has become an essential approach in pharmaceutical analytical method development. Instead of relying only on end-product testing, AQbD focuses on designing quality into analytical methods using scientific understanding and risk-based principles.
This webinar explains how AQbD supports:
- Robust analytical method development
- Better regulatory compliance
- Improved analytical performance
- Lifecycle management of analytical methods
- Efficient pharmaceutical quality systems
About the Webinar
The webinar will explain how AQbD principles align with modern International Council for Harmonisation (ICH) Guidelines.
Participants will learn practical approaches for:
- Analytical method development
- Method optimization
- Risk assessment
- Design of Experiments (DoE)
- Method robustness
- Regulatory compliance
- Lifecycle management
The session is designed to bridge academic concepts with real-world pharmaceutical applications.
What You Will Learn
Participants will gain knowledge about:
- Fundamentals of Analytical Quality by Design (AQbD)
- Quality by Design (QbD) principles
- Integration of AQbD with ICH Guidelines
- Analytical method development strategies
- Design of Experiments (DoE)
- Quality Risk Management (QRM)
- Critical Method Attributes (CMAs)
- Method robustness evaluation
- Lifecycle management of analytical methods
- Industrial applications of AQbD
Key Topics Covered
| Topic | Description |
|---|---|
| AQbD Fundamentals | Scientific approach to analytical quality |
| ICH Guidelines | Regulatory framework for analytical methods |
| Analytical Method Development | Designing reliable analytical procedures |
| Design of Experiments (DoE) | Statistical optimization techniques |
| Quality Risk Management | Risk-based analytical development |
| Critical Method Attributes | Performance parameters for analytical methods |
| Lifecycle Management | Continuous improvement of analytical methods |
| Industrial Applications | Practical implementation in pharmaceutical industries |
Speaker Profile
Dr. Bikash Ranjan Jena is an Associate Professor in the Department of Pharmaceutical Analysis at The Neotia University (Ambuja Neotia Group), West Bengal.
He has extensive experience in:
- Pharmaceutical Analysis
- Analytical Method Development
- AQbD Research
- Pharmaceutical Education
- Regulatory Science
During this webinar, he will share practical insights into implementing AQbD in accordance with international regulatory standards.
Why Should You Attend?
By attending this webinar, participants will:
- Understand AQbD principles
- Learn modern analytical method development
- Gain knowledge of ICH Guidelines
- Improve pharmaceutical analytical skills
- Explore industrial applications of AQbD
- Strengthen regulatory understanding
- Stay updated with current pharmaceutical trends
Who Should Attend?
This webinar is ideal for:
- B.Pharm Students
- M.Pharm Students
- Pharm.D Students
- Ph.D. Scholars
- Pharmaceutical Researchers
- QA Professionals
- QC Professionals
- Analytical Scientists
- Regulatory Affairs Professionals
- Faculty Members
- Pharmaceutical Industry Professionals
Organising Committee
The webinar is coordinated by the UPHAR Foundation, Odisha team.
| Role | Name |
|---|---|
| Convenor | Dr. Chinmaya Sahoo |
| Joint Convenor | Mr. Sourav Biswal |
| Tech Guru | Mr. Sajan Sahoo |
| Coordinator | Miss Bandita Biswal |
| Host | Mr. Chirag Goyal |
| Co-Coordinator | Mr. Satya R. Dash |
| Certification Coordinator | Mr. Kulamani Sagar |
| Registration Coordinator | Mr. Santosh Pradhan |
Why Pharmacy Students Should Attend
Understanding AQbD is becoming increasingly important for careers in pharmaceutical research, quality assurance, regulatory affairs, and analytical development.
This webinar helps students:
- Build industry-relevant analytical skills
- Understand regulatory expectations
- Prepare for GPAT, NIPER, and higher studies
- Improve research methodology
- Learn current pharmaceutical industry practices
Registration Information
Interested participants can register free of cost before the webinar.
| Particular | Details |
|---|---|
| Registration | Free |
| Platform | Google Meet |
| Mode | Online |
| Certificate | Not mentioned in the official announcement |
Important Dates
| Event | Date |
|---|---|
| Webinar Date | 1 November 2026 |
| Time | 11:30 AM – 12:30 PM (IST) |
Important Links
| Link | Status |
|---|---|
| Registration Link | Available through the official organizer |
| Official Organizer | UPHAR Foundation, Odisha |
Conclusion
The AQbD Webinar 2026 is an excellent learning opportunity for pharmacy students, researchers, academicians, and pharmaceutical professionals who want to strengthen their understanding of Analytical Quality by Design (AQbD) and ICH Guidelines.
With expert guidance from Dr. Bikash Ranjan Jena, participants will gain practical insights into analytical method development, Quality by Design principles, risk management, and regulatory expectations. Anyone interested in pharmaceutical analysis and quality systems should consider attending this free national webinar.
Frequently Asked Questions (FAQs)
Q1. What is the AQbD Webinar 2026?
The AQbD Webinar 2026 is a free online educational webinar organized by UPHAR Foundation, Odisha, focusing on Analytical Quality by Design (AQbD) and its integration with ICH Guidelines.
Q2. Who is the speaker for this webinar?
The webinar will be delivered by Dr. Bikash Ranjan Jena, Associate Professor, Department of Pharmaceutical Analysis, The Neotia University.
Q3. When will the webinar be held?
The webinar is scheduled for Sunday, 1 November 2026, from 11:30 AM to 12:30 PM (IST).
Q4. Is there any registration fee?
No. Registration for the webinar is completely free.
Q5. Which platform will be used for the webinar?
The webinar will be conducted on Google Meet.
Q6. Who can attend this webinar?
B.Pharm, M.Pharm, Pharm.D students, Ph.D. scholars, researchers, QA/QC professionals, analytical scientists, regulatory affairs professionals, faculty members, and pharmaceutical industry professionals can attend.
Q7. What topics will be covered?
The webinar includes AQbD fundamentals, ICH Guidelines, Design of Experiments (DoE), Quality Risk Management, Critical Method Attributes, analytical method development, and lifecycle management.
Q8. Will participants receive a certificate?
Not mentioned in the official announcement.
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