Industries, commented, "QbD is a systemic approach to product development whereby manufacturers should have a ready blueprint of their products before commencing work on the actual development which reflects the complete understanding of product and process with in-depth knowledge, science, experience and technical soundness. QbD can change the efficiency of manufacturing from low to high and provide most the reliable, reproducible and robust manufacturing process. QbD can minimise waste as QbD evokes trial and error approach. QbD provides the opportunity of technology innovation with less technical and financial risk."
The must-attend event will help attendees get an overview of overall opportunities and challenges in implementing QbD and a in-depth workshop to guide attendees on implementing QbD. The agenda is specifically designed for those in the research and development, formulation, analytical, quality control, quality assurance and regulatory working in pharmaceuticals, as well as organisations and institutions that devote the majority of their efforts to research, development, technology transfer, or commercialisation of pharmaceuticals.
For more information about CPhI -- Quality by Design, please visit: http://www.qualitybydesign-asia.com
CPhI Conferences deliver the latest pharma market insight, in-depth case studies and exceptional networking opportunities through a programme of high-level conferences. The worldwide series of events, spanning four continents, provides the optimum forum for you to learn, make new business connections and identify the latest growth opportunities.
Delivered by expert teams in each region, every conference is extensively researched with leading professionals, ensuring that CPhI Conferences tackle the most business critical issues facing the pharma industry today.
For more information about CP
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