Good Laboratory Practice 1 - GLP Training (GLP01)
This one day GLP course is updated regularly to provide clients with current GLP trends and information. This course is designed for staff working in the early phase drug development and commercial operations.
For example;
- Quality Assurance / Quality Control personnel
- Laboratory personnel
- People new to the GxP regulated industries
As the FDA states; “Each individual engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have education, training, and experience, or combination thereof, to enable that individual to perform the assigned functions.” – Subpart B-Organization and Personnel
Learning Objectives and Course Description
This course includes:
- understand the basics of GLP and basic good documentation practice
- No White out / How to strike out errors etc
- be able to adopt GLP requirements into their day to day work tasks
- have a relevant working knowledge of GLP
- have a relevant working knowledge of the ISO 17025 and OECD GLP principles
- the basic principles of the OCED GLP regulations
- adopt the GLP requirements into their day to day work tasks and non-clinical projects
- understand the intent of the OECD GLP Principles
- a relevant, working knowledge of the OECD GLP principles
- participate in GLP studies and know the roles and functions of key personnel within a study
- develop GLP compliant documentation
- the Quality Assurance Unit and its role in GLP
- management responsibilities in a GLP context
This one day course is intended to provide participants with a working knowledge (illustrated by recent examples) and understanding of the current cGMP.
Benefits include
- learning from experienced professional skilled trainers
- understanding GLP and its application to all personnel
- skilled people means less errors and improved profitability for your laboratory
- one on one tuition during the course as the classes and are small and intimate
- receipt of a complete training kit, trainer’s notes and a certificate of completion for participants assessed.
View schedule and how to make a booking.
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