Life Sciences
Maintenance Excellence
This course examines in detail at the requirements for Maintenance Excellence
Downstream Bioprocessing
Provides the learner with an insight into the various stages of processing that occur after the completion of the fermentation or bioconversion.
Upstream Bioprocessing
Provides the learner with an insight into the stages of microorganism growth required to produce biopharmaceuticals.
Introduction to Bioprocessing
This course introduces the processes involved in making useful products such as pharmaceuticals, materials, food and energy from living cells or their components.
Lean Six Sigma (Green Belt)
Will help you be able to deploy improvement tools, analyse data and identify appropriate situations, goals and team members for Kaizen events.
Maintaining Improvements
For those who want to learn about applying and maintaining Continuous Improvement in their work and who may have little or no previous experience in this area
Quality Improvement
For those who want to learn the basics of Quality Improvement in manufacturing or business processes, and who may have little or no previous experience in this area.
Lean and Waste Reduction
Equips the learner with the skills and competencies to appreciate the development of Lean concepts and to utilise a range of waste reduction tools.
Continuous Improvement in Manufacturing (Intro)
Equips the learner with the skills and competencies to utilize a range of continuous improvement methodologies whilst working in the manufacturing sector.
Packaging for Life Science Products
Provides the learner with an insight into the purpose and types of packaging and labels.
Infection Control
Understand the key systems and practices of infection prevention and control that should be implemented by management and staff to prevent patients and health workers from being harmed by avoidable infections.
Personnel in the Cleanroom
In this course we detail the personal behaviours and practices that will help to minimize these contamination risks.
Cleanroom Validation
Examines the concept of validation, the principles of clean-room validation and how validation is planned, executed and maintained.
Cleaning, Sterilisation & Aseptic Practice
Examines how cleaning, sterilization and aseptic practice is best implemented in the clean-room. We’ll explain how cleaning, sterilization and aseptic practice takes place.
Cleanroom Design
Understand the regulatory guidelines for cleanroom design and the factors that impact design. Understand how HVAC, airlocks, filters and construction materials are used to prevent contamination.
Cleanroom Micro-organisms
Provides an introduction to the world of microbiology and the impact it has on the cleanroom environment.
Introduction to Cleanroom Operations
Provides an overview of cleanroom operation. You’ll learn about the need from cleanrooms, their classification and contamination control.
Good Manufacturing Practice (GMP)
Understand the principles and operating practices that need to be followed for companies to manufacture Life Science products in compliance with the regulations, codes of practise and guidelines that apply.
