Pharma Quality Systems 2025
10 - 12 June - In Person
Foundation knowledge area of the QP Study Guide
You are already an expert in PQS - take your knowledge and understanding to the next level...
By the end of this module, you will have a comprehensive knowledge of the systems required to support the oversight and control of the manufacture, testing and distribution of a medicinal product, throughout its lifecycle by implementing robust a Pharmaceutical Quality System
Philosophy and principles of Quality Assurance, Quality Management across organisations
Design of Quality systems appropriate to lifecycle stage and activities performed
Principles of Quality Risk Management, including hazard identification and risk mitigation, including where it can be utilised
Key Elements of Pharmaceutical Quality Systems, including:
# Quality Management infrastructure
# Production planning / scheduling and capacity planning, Vendor assurance including audits and technical agreement
# Product Quality Reviews
# Supply chain oversight
# Design, control, validation of premises, equipment and utilities
Key interpersonal skill for the QP
Your materials, assignments and assessments will all be provided through this learning portal
You will be notified by email when items are available for you to access...
1 month before the course start date
~ You can access your course workbook
~ You will be able to download your Preparatory Assignment
Day before course start date
~ Downloads for workshops and exercises
End of each course day
~ Answers to exercises where appropriate
After course
~ Learning assessment
~ Course evaluation
~ Certificate
Location: Maidstone Innovation Centre
Gidds Pond Way,Weavering, Maidstone, Kent ME14 5FY
Call us directly on
01622 477781
email us
[email protected]
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