ISO 22716:2007 Cosmetics - Good Manufacturing Practices (GMP) Introduction Training Course
Through a series of discussion-based sessions and interactive workshops, learn how to help your organisation demonstrate Good Manufacturing Practice (GMP) compliance using ISO 22716. Build a strong foundation of knowledge and skills.
Course Overview
What you'll learn
- Discuss and interpret all clause requirements of ISO 22716
- Identify production process issues to be addressed in accordance with the standard
- Identify requirements for manufacturing and quality documentation
- Analyse real-world situations to identify opportunities for continual improvement, in accordance with the standard
Who This Course Is For
Those involved in the development, implementation and management of good manufacturing practices for cosmetic products. The course will benefit those planning to complete other GMP training, such as internal auditor.
NOTE: Learners are required to obtain a copy of the ISO 22716:2007 Cosmetics – Good Manufacturing Practices Standard. Learners should familiarise themselves with the standard prior to attending the training course.
Virtual Course requirements:
To ensure your access to the virtual course and to gain the most out of this training we request all learners have:
- Reliable internet access (High speed)
- Computer with microphone and camera capabilities
Assessment and group activities for this course requires your camera to be turned on. Background effects such as blurring can be used for preserving privacy.
About this course
Through a series of discussion-based sessions and interactive workshops, learn how to help your organisation demonstrate Good Manufacturing Practice (GMP) compliance using ISO 22716. Build a strong foundation of knowledge and skills.
Course Topics:
- Overview of GMP and the Standard
- Clause 3: Personnel Requirements
- Clause 4 and 5: Premises and Equipment Requirements
- Clause 6 and 12: Raw and Packaging Materials including subcontracting Requirements
- Clause 7 and 8: Production and Finished products requirements
- Clause 9: Quality Control Laboratory requirements
- Clause 10, 11 and 13: Treatment of product that is out of specification including Deviations and Waste management requirements
- Clause 14: Complaints and recalls requirements
- Clause 15 and 17: Change Control and Documentation requirements
- Clause 16: Internal audit requirements
- Learning Review and Summary
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