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Training & Seminars

Module 1 – International Good Manufacturing Practices, Quality Management Systems and GMP for Pharmaceutical Operations (23 – 25 January 2018) – 3 day Course

Dari Selasa, 23 Januari 2018 -  8:00
Ke Khamis, 25 Januari 2018 -  5:00

Aim: To provide an introduction to the regulations and Codes of Practice that governs the manufacture of therapeutic goods bothnationally and internationally. To develop a broad understanding of the scope of Good Manufacturing Practices and Quality Management Systems applicable to drugs, devices and biologics and to provide a detailed analysis of the GMP requirements for manufacturing pharmaceuticals.


Day 1
AM ►QA Principles & International GMPs, updates of ASEAN Harmonisation focusing on GMP
PM ►Quality Management, Quality Assurance & Quality Control

AM ►Key Quality Assurance Systems and GMP Responsibilities for Managers & Supervisors
PM ►GMP Principles for Manufacturing Operations

Day 3
AM ►GMP Principles for Packaging Operations includes control of printed packaging materials, line clearance and reconciliation of materials/products
AM ►GMP Principles for Warehousing (related to manufacturing)
PM ►Equipment Management