Vispact Consulting delivers tailored engineering and management solutions for the life sciences industry. From project engineering to organizational transformation, we partner with you to drive sustainable growth and compliance.
Quality & Compliance
In pharma and biotech, the smallest detail can make the biggest difference. A system not validated, a record not aligned, or a utility not qualified — and suddenly, timelines slip, approvals stall, and patient trust is at risk. Compliance isn’t just a requirement; it’s the heartbeat of safe, reliable operations.
Too often, companies treat compliance as a checklist exercise. But when regulations evolve faster than processes, gaps appear. These gaps can turn into audit findings, delayed approvals, or worse — threats to patient safety. The pressure is relentless, and the cost of failure is high.
Where Vispact Steps In
We don’t just tick boxes; we engineer compliance into the DNA of your operations. Our quality & compliance services cover systems, equipment, and facilities — ensuring every element is designed, qualified, and validated to GMP standards from day one. Whether it’s a new production line, a digital system rollout, or an existing facility upgrade, we deliver audit-ready reliability, every time.
Our Specialized Services
Computer System Validation (CSV)
Modern pharma runs on digital platforms — but without validation, those platforms are vulnerable.We provide full-lifecycle CSV support: from defining requirements and assessing risk to executing validation and preparing documentation. Aligned with GAMP 5 and international standards, we ensure your systems deliver data integrity, reliability, and audit confidence.
Qualification & Validation (QV)
Every piece of equipment, every utility, every facility has to prove itself before it can be trusted. Our experts design risk-based QV strategies across DQ, IQ, OQ, and PQ phases. The outcome? Smooth startups, minimized downtime, and operations that stay compliant without slowing production.
Commissioning & Decommissioning
Beginnings and endings matter. Commissioning a new facility without proper controls can delay launch. Decommissioning without compliance can create risk long after shutdown.We manage both with precision — from documentation and testing at startup to safe, compliant phase-out at closure. The result: lower risk, lower cost, and complete regulatory peace of mind.
Compliance isn’t just about avoiding risk.
It’s about building trust. Let’s make it your competitive edge.
Vispact Consulting delivers tailored engineering and management solutions for the life sciences industry. From project engineering to organizational transformation, we partner with you to drive sustainable growth and compliance.
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