Global Pharma Validation Checklist: Stay FDA-Ready with Inotek
Автор: Inotek – Pharma Facility Experts
Загружено: 2025-12-23
Просмотров: 7
Pharma validation is no longer just a local task — it’s a global responsibility. In today’s fast-evolving pharmaceutical landscape, facilities must meet a broad range of regulatory standards, including FDA, GMP, ISO 14644, and more, with no room for error. In this video, we dive into the six critical steps that ensure your pharma facility is audit-ready, compliant, and inspection-ready every time.
We explore:
The importance of clear user requirements and risk management.
How facility design impacts compliance, from cleanrooms to data integrity.
The role of disciplined execution in sustaining inspection readiness throughout the facility’s lifecycle.
At Inotek, we are recognized as a Top 10 Pharma Turnkey Contractor & Project Consultant (2022 & 2025), known for our expertise in integrating compliance, engineering, and execution from the ground up. With our global insight into pharma project management, we help clients build facilities that not only meet expectations but exceed them — ensuring continuous compliance across audits and inspections.
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