Training & seminars
Module 1 – International Good Manufacturing Practices, Quality Management Systems and GMP for Pharmaceutical Operations (23 – 25 January 2018) – 3 day Course
23 January 2018 – 25 January 2018
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
Day2
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