Our philosophy on validation combines practicality and compliance. We design, develop and execute programs that help you qualify YOUR equipment and validate YOUR processes and not those of another company. Our unique bottom-up approach to validation consists in learning and understanding your operational needs in order to validate only those activities that are relevant to you, so that your equipment gets qualified for its intended use and your processes get validated to meet regulatory requirements. We intervene at various levels of your projects and offer validation activities that include
- Documentation Preparation (VMP, CVMP, CSVMP)
- IOQ/PQ design, execution and reporting
- Periodic qualification, ongoing validation and re-certification
QUESTIONS ABOUT A PHARMACEUTICAL ISSUE? ASK OUR EXPERTS.
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