Life Sciences

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Maintenance Excellence

This course examines in detail at the requirements for Maintenance Excellence

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Downstream Bioprocessing

Provides the learner with an insight into the various stages of processing that occur after the completion of the fermentation or bioconversion.

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Upstream Bioprocessing

Provides the learner with an insight into the stages of microorganism growth required to produce biopharmaceuticals.

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Introduction to Bioprocessing

πŸ“œ CPD Certified

This course introduces the processes involved in making useful products such as pharmaceuticals, materials, food and energy from living cells or their components.

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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.

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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

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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.

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Lean and Waste Reduction

πŸ“œ CPD Certified

Equips the learner with the skills and competencies to appreciate the development of Lean concepts and to utilise a range of waste reduction tools.

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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.

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Packaging for Life Science Products

πŸ“œ CPD Certified

Provides the learner with an insight into the purpose and types of packaging and labels.

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Infection Control

πŸ“œ CPD Certified

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.

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Personnel in the Cleanroom

πŸ“œ CPD Certified

In this course we detail the personal behaviours and practices that will help to minimize these contamination risks.

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Cleanroom Validation

πŸ“œ CPD Certified

Examines the concept of validation, the principles of clean-room validation and how validation is planned, executed and maintained.

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Cleaning, Sterilisation & Aseptic Practice

πŸ“œ CPD Certified

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.

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Cleanroom Design

πŸ“œ CPD Certified

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.

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Cleanroom Micro-organisms

πŸ“œ CPD Certified

Provides an introduction to the world of microbiology and the impact it has on the cleanroom environment.

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Introduction to Cleanroom Operations

Provides an overview of cleanroom operation. You’ll learn about the need from cleanrooms, their classification and contamination control.

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Good Manufacturing Practice (GMP)

πŸ“œ CPD Certified

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.