Deviations Process - Practitioner
Course Description:
In the cosmetics manufacturing industry, it is crucial to address deviations in a systematic and organised way to ensure the quality, safety, and effectiveness of cosmetic products. It is therefore essential for employees involved in managing deviations across all departments to have a comprehensive understanding of the process, as well as the importance of adhering to timelines for managing deviations. This training course also emphasises the significance of risk assessment and conducting a thorough root cause analysis to determine appropriate corrective and preventive actions. By the end of this course, employees will gain a deeper understanding of how to identify and manage deviations to ensure compliance with Good Manufacturing Practices (GMP) and maintain product integrity.
Learning Outcome:
- Understand the deviation process in cosmetics manufacturing
- Classify deviations into various types specific to cosmetics production
- Outline the root cause analysis process for cosmetic product deviations
- Explain the risk assessment process in cosmetics manufacturing
- Define Corrective Action and Preventive Action (CAPA) and how they are initiated in cosmetics production
- Detail the process for closing out a deviation in the cosmetics industry
- Understand the deviation process in cosmetics manufacturing
- Classify deviations into various types specific to cosmetics production
- Outline the root cause analysis process for cosmetic product deviations
- Explain the risk assessment process in cosmetics manufacturing
- Define Corrective Action and Preventive Action (CAPA) and how they are initiated in cosmetics production
- Detail the process for closing out a deviation in the cosmetics industry
Course Features
| Modules | : | 1 |
| Duration | : | 1 Hour(s) |
| Language | : | English |
| Assessment | : | Self |
| Skill Level | : | Entry |
Course Content(s)
Deviations Process - Practitioner (CPDV0202)
This module will focus on the process of dealing with deviations in a systematic way in a GMP environment. It gives details on how to raise, manage and review them including finding the root cause and finding the corrective actions and preventative actions to avoid recurrence.