The new EU GMP Annex 1 draft, Rev 12 specifies the requirements of a pharmaceutical risk assessment to set appropriate microbiological plate conditions. This blog discusses this requirements to use a risk assessment, and then provides an interpretation on how to apply it and use it in different stages of the manufacturing process.
There are three main concepts regarding this:
- “Quality Risk Management” applies to all of Annex 1 and is the underlying concept for understanding and interpreting Annex 1.
- A relevant Pharmaceutical Risk Assessment is expected for each area.
- Companies are expected to implement a Quality Assurance system to fulfill the quality objectives associated with various areas of interest
Section 9 of Annex 1 says that a Risk Assessment should be used to establish a comprehensive environmental monitoring program, including:
A pharmaceutical Risk Assessment should be based on knowledge of:
- historical monitoring data
- monitoring data obtained during qualification
- knowledge of typical microbial flora isolated from the environment
The result of the Risk Assessment is to establish the most appropriate incubation conditions to identify all potential microorganisms associated with an environment. That is, the goal is to demonstrate that your methods have considered all risks for maximum recovery of microorganisms. This is particularly important in Grade A and B Cleanrooms where the counts are generally very low, and the environmental conditions do not favor microbiological detection.
- Establish the most appropriate incubation conditions to identify all potential microorganisms associated with your environment
- Take information from USP and EU Pharmacopeia
- Risk Assessment: Evaluate the environment and process/product
- Risk Assessment: Review data regularly to confirm the effectiveness of the conditions
A Pharmaceutical Risk Assessment should be holistic and evaluate the characteristics of the process, products, facilities and environmental conditions that favor the growth of:
- anaerobic microorganisms
- slow-growing microorganisms
- yeasts and molds
There are differences in performing a Risk Assessment in existing or new departments. For example, in existing departments, there is historical data would should be considered. In a new department with no historical information, you must define the incubation condition based on a scientific-based approach:
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Visit our Annex 1 page or read more of our Annex 1 blogs:
- Cleanroom Classification, Cleanroom Monitoring, Cleanroom Qualification per Annex 1
- Cleanroom Process Risk Assessment per Annex 1
- Cleanroom Sampling Points
- Viable Non Viable Particle Counts
- Contamination Control Strategy
- Quality Risk Management
- Cleaning & Disinfecting a Cleanroom per Annex 1
- Cleanroom Single Use Requirements per Annex 1