Abstract
This paper presents a practical way in which current approaches to quality risk management (QRM) may be improved, such that they better support qualification, validation programs, and change control proposals at manufacturing sites. The paper is focused on the treatment of good manufacturing practice (GMP) controls during QRM exercises. It specifically addresses why it is important to evaluate and classify such controls in terms of how they affect the severity, probability of occurrence, and detection ratings that may be assigned to potential failure modes or negative events. It also presents a QRM process that is designed to directly link the outputs of risk assessments and risk control activities with qualification and validation protocols in the GMP environment.
Original language | English |
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Pages (from-to) | 243-261 |
Number of pages | 19 |
Journal | PDA journal of pharmaceutical science and technology |
Volume | 66 |
Issue number | 3 |
DOIs | |
Publication status | Published - May 2012 |
Keywords
- Change control
- Controls
- Good manufacturing practice
- Qualification
- Quality risk management
- Subjectivity
- Uncertainty
- Validation