Implementing ISO 22716 GMPs: Best Practices for Cosmetics Manufacturers
Learn the guidelines for good manufacturing practices (GMPs) regarding personnel health and hygiene, raw materials, packaging materials, manufacturing sites (including the quality control laboratory), waste management, documentation, and more.
Overview
Gain an understanding of current good manufacturing practices, or GMPs, for cosmetic products. It will explain the requirements in ISO 22176, “Guidelines on Good Manufacturing Practices” and provide practical information on implementing processes and practices that meet the requirements and enable you to produce a product that meets quality and safety requirements.
Each section of the training will explain the requirements and valuable practical information on the topic. After the information is provided the student will complete an exercise section that gives an opportunity to work with and reinforce the information.
Expertly detailed in this course are guidelines to maintain product quality across categories, such as:
- Premises and equipment requirements
- Raw materials and packaging materials
- Out-of-specification criteria and deviations
- Complaint and recall procedures
The subject material is delivered in a digestible, straightforward style suitable for most learning levels and styles. Each section has an assessment at the end which a user must pass with an 80% or higher to move on to the next section. There is no final assessment. This course is suitable for managers and supervisors at a cosmetic manufacturing site.
Agenda
1. Section 1-2: Scope, Terms, and Definitions
2. Section 3: Personnel
3. Section 4: Premises
4. Section 5: Equipment
5. Section 6: Raw Materials and Packaging Materials
6. Section 7: Production
7. Section 8: Finished Products
8. Section 9: Quality Control Library
9. Section 10: OOS Products
10. Section 11: Waste
11. Section 12: Subcontracting
12. Section 13: Deviations
13. Section 14: Complaints and Recalls
14. Section 15: Change Control
15. Section 16: Internal Audit
16. Section 17: Documentation