Validation

At VPS, regulatory compliance is central to achieving operational excellence within the pharmaceutical, biotechnology, and life sciences industries. Our dedicated CQV specialists have extensive knowledge and practical experience with current industry standards, including cGMP, GAMP 5. This expertise ensures your facility maintains consistent, repeatable compliance with pharmaceutical validation and qualification requirements.

We adopt a collaborative approach, working closely with your internal quality teams and facility stakeholders from the earliest stages of your project. Our proactive planning clearly defines CQV strategies from the outset, effectively managing critical milestones and dependencies, providing transparency throughout, and accelerating your facility’s readiness. Our structured methodology integrates industry-leading project management practices, lean techniques, and rigorous scientific risk assessments to optimise cost-effectiveness and ensure timely project delivery.

At VPS, commissioning is a comprehensive process that blends thorough technical know-how with practical, hands-on experience. Our diverse team, composed of mechanical, electrical, automation, process, and commissioning professionals, works collaboratively to ensure your facility is operational, efficient, and compliant from the outset. Early identification and resolution of potential challenges during commissioning significantly reduce ongoing operational and maintenance expenses.