3-Day International Masterclass on Formulation Development & QbD: “From Concept to Lab Bench” to Empower Researchers and Pharmacy Educators

Springwell Pharma Private Limited is set to organize a 3-Day International Masterclass on Formulation Development, Quality by Design (QbD), and Advanced Pharmaceutical Research, titled “From Concept to Lab Bench”, scheduled from 20 to 22 January 2026. The online masterclass will be conducted via Google Meet from 7:00 PM to 8:30 PM IST, catering specifically to researchers, pharmacy teachers, academicians, and pharmaceutical professionals.

The masterclass aims to bridge the gap between theoretical concepts and practical laboratory applications in pharmaceutical formulation development. With a strong focus on QbD principles, risk assessment, design of experiments (DoE), and regulatory perspectives, the program is designed to enhance both academic understanding and industry-oriented skills.

Eminent Speakers

The event will feature distinguished experts from academia and industry:

Dr. Bhupinder Singh Bhoop – Honorary Professor at Panjab University, Professor Emeritus at Chitkara University, and a pioneer of QbD in India, who brings decades of expertise in pharmaceutical sciences and regulatory quality frameworks.
Dr. Pranav Shah – Principal and Professor (Pharmaceutics), DCVP College of Pharmacy, Uka Tarsadia University, known for his contributions to formulation science and academic leadership.
Dr. Khushwant Yadav – Associate Professor at SPP SPTM, SVKM’s NMIMS, with academic and postdoctoral experience from the USA, contributing insights into modern pharmaceutical research and innovation.

Key Learning Outcomes

Participants will gain in-depth knowledge and practical insights into:

Formulation and Pre-formulation Science, including dosage form strategy, excipient selection, FTIR, DSC, and essential preformulation tools.
Quality by Design (QbD) and Risk Assessment, covering QTPP, CQA, Fishbone diagrams, FMEA, and interpretation of ICH Q8–Q11 guidelines.
Design of Experiments (DoE) and Design Space, focusing on statistical design, input–output mapping, and optimization strategies.
Trial Evaluation and Scientific Reporting, including batch evaluation, stability studies, project documentation, and data presentation.
Patents and Innovation Pathways, guiding participants through patent filing processes, novelty criteria, and research-to-IP transitions.

Registration Details

The registration fee is ₹1000, with an early bird offer of ₹900. Upon successful completion, participants are expected to gain enhanced competency in formulation development and regulatory-aligned research practices, making the masterclass highly beneficial for both teaching and industrial research careers.

This initiative by Springwell Pharma reflects its commitment to advancing pharmaceutical education, research excellence, and innovation by providing a global learning platform led by renowned experts.

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