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Nova Cleaning Validation - Version NOVA-CVM -Automated Cleaning Validation and Risk Management Software
A holistic and process-specific risk mitigation system. Nova-Cleaning Validation significantly enhances product integrity by managing changes and assessing the risks associated with cross-contamination and product impurities within a dynamic production environment. All changes to methods, APIs, products, equipment, and family groups are automatically evaluated to ensure product integrity and regulatory compliance. Nova-Cleaning Validation complies with 21 CFR Part 11 and EU Annex 11. The system uses a risk-based approach and is designed based on PDA Technical Reports 29 and 49, ISPE MaPP, 21 CFR Part 211.67.
Computerized worst case evaluation. Risk factors including dosage, toxicity, cleanability, solubility and more can be defined together or separately, allowing the user to have complete control over the evaluation settings. The worst case is determined and displayed for all validation groups, enabling users to focus on the biggest risk to product quality. The worst case assessment is automatically triggered when any validation group property is changed. Fully automated
MAC calculations. Carryover limits are calculated for all sample points for APIs, cleaning agents, and microbial testing. Hundreds of MAC formulas are executed in seconds, rather than hours. The calculations take into account all possible product A and product B combinations for the affected equipment trains and validation groups, and the lowest MAC values are highlighted, making user review of the calculated values quick and easy.
The process dedicated change evaluation feature consolidates the impact of multiple changes in one snapshot of the risks and consequences of potential changes to any factor that may affect the validated state of the cleaning process. These factors include changing equipment, introducing new products, modifying batch sizes, and anything else that relates to both the product and equipment families that are part of equipment trains and validation groups.
- Fast ROI providing significant time savings over manual processes
- Data Security with 21 cfr 11 Part 11 compliance
- Reduced Error with a totally paperless system
- Efficiency through electronic management and approval of master data.
- System Defined Protocols with sampling plans that are automatically generated for validation groups
- Comprehensive Reporting enables users to quickly retrieve in-depth standard reports and statistical analysis