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This Guide is the first in a series of ISPE Product Quality Lifecycle Implementation (PQLI®) Good Practice Guides (GPGs) that will describe enhanced, quality by design approaches to product realization, and is an introduction to and an overview of the Guides Series. Product realization is the achievement of a product with the quality attributes appropriate to meet the needs of patients, health care professionals, regulatory authorities (including compliance with marketing authorization), and internal customers’ requirements.
This Overview Guide and the subsequent ISPE PQLI GPG Series address product and process development, transfer to, and establishment of, commercial manufacture using science- and risk-based approaches. Other Guides in the Series will cover:
The Guide uses ICH Guidelines Q8 (R2), Pharmaceutical Development, Q9, Quality Risk Management, and Q10, Pharmaceutical Quality System as a basis, together with other relevant ICH Guidelines.
Know Before You Go: Process Validation Conferences
Friday, 21 Oct 2016 12.10
Chairman’s Chatter: Collaboration
Thursday, 20 Oct 2016 14.10
Moving to Single-Use Continuous Manufacturing
Wednesday, 19 Oct 2016 12.10