Cleaning, Sterilization and Process Validation
Our consultants have experience in validating a majority of the systems found in the Pharmaceutical, Biotech and Medical Device Industry. Innovative Engineering Consulting Group has the expertise to develop validation strategies, master plans, protocols, and final reports.
We have hands-on experience to validate utilities, process equipment and computers/automation systems. We can also help you in supporting the validation of your process. Based on specific needs, Innovative Engineering Consulting Group is able to customize a value added approach which may entail strategic expertise, project execution, third party auditing services or/and staff augmentation.
- Validation Strategies and Development of Validation Programs
- Process Validation Master Plans, PPQ Protocols and Summary Reports write-up/review
- Cleaning Validation protocol development and execution
- Steam Sterilization protocol development and execution
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