Module 9 - Solid Dose Manufacture Pri...
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Module 9 – Solid Dose Manufacture Principles and Practices
Upcoming Events & Interviews
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Aim: To provide an introduction to the GMP requirements for the formulation, scale up and optimization of Finished Dose Forms, and to develop a practical understanding of Process Mapping, Risk Analysis and Critical Control points, Validation requirements and Quality Plans as it applies to solid dose formulations. Organised by Malaysian Organisation of Pharmaceutical Industry together with Seer Pharma and National Pharmaceutical Control Bureau. Date: 24 – 26 Nov 2015

Day 1

AM ►QA/GMPs Over Finished Dose Forms (FDF)

PM ►Granulation Technology & Control

Day 2

AM ►Blending and Milling Technology & Control

PM ► Encapsulation Technology and Control

Day 3

AM ► Compression Technology and Control

PM ►Coating Technology & Control



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