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About PAT and QbD

Maintaining quality has always been imperative for the healthcare industry to protect the safety of patients and consumers. It is rare to see discussion of future of pharmaceutical manufacturing without using the terms Quality by Design (QbD) and Process Analytical Technologies (PAT).

PAT & Qbd goes hand in hand with each other.. It has been seen with the adoption of QbD and PAT principles for a new product development makes sense not only from the regulatory compliance perspective, but also make sense for financial reasons. They certainly complement each-other and the likelihood is that the partnership has a very promising future. This workshop will focus on discussing the existing challenges and explore practical applications related to drug development, manufacturing and regulatory. It’s a 2-day program which will include presentations, talks, case studies, panel discussions from industry leaders, solution providers and academia.

Key Features
Panel Discussion
Case Studies
Benefits of Attending
Understand the guidelines and regulatory expectations
Enhance the skills and knowledge on DoE
Economics of PAT & QbD to fast-track production and approvals thereby minimizing product recalls and prevent warning letters
Gain insights on statistical tools and risk-based approach
Tech-transfer and Continuous improvement Process Verification along with validation lifecycle approach
Techniques for better industry – academia collaboration
Learn strategies for successful implementation of PAT and QbD techniques in Continuous manufacturing and API processes
Pharmaceuticals Life sciences Bio-Pharmaceuticals
Process Engineers Research and Development QA Product Development
  • Vice Presidents
  • Associate Vice Presidents
  • Directors
  • Associate Directors
  • Deputy General Manager
  • Principal Engineer
  • General Manager
  • Senior Managers
  • Managers
  • Assistant Managers
  • Senior Executives
Platinum Partner
Gold Partner
Silver Partner