One Day State-Level Symposium on Quality by Design & Regulatory Compliance

Department of Pharmaceutics, Faculty of Pharmacy, RUAS organized one day state level symposium on “Quintessentials of Quality by Design and Regulatory Compliance in Pharmaceutical Product Life Cycle” highlights the modern shift in drug development and manufacturing. Quality by Design (QbD) is a proactive approach that embeds quality into products from the outset, focusing on predefined objectives, scientific understanding, and risk management rather than relying solely on end-product testing.

The core elements of QbD include defining the Quality Target Product Profile (QTPP), identifying Critical Quality Attributes (CQAs), determining Critical Process Parameters (CPPs) and establishing a robust control strategy. Together, these ensure consistent product development till withdrawal of product from the market quality.

Aligned with global regulatory frameworks (USFDA, EMA), QbD supports efficient approvals and lifecycle management by demonstrating strong process understanding. This integration of quality and compliance safeguards patient safety and product efficacy throught the entire pharmaceutical product lifecycle.

Event Details:

Event Date: 22.11.25

Event Time: 10 Am onwards

Event Venue: Lecture Hall 01, 3rd Floor, Faculty of Pharmacy

Chief Guest: Dr. Santanu Roy, Dr Mahesh B K, Mr. Santosh Kashyap, Ms. Kalpana N