Independent Validation
About
Veridatum is an independent pharmaceutical validation consultancy. We execute qualification protocols, certify data integrity systems, and prepare organisations for regulatory inspection. We exist because pharmaceutical companies deserve a voice separate from their vendor confirming that their infrastructure meets FDA, EMA, and ICH standards.
Not the vendor's word. Ours.
Traditional validation costs $150K–$300K in consulting fees and takes 6–12 months. We reduce that to days.
01
IQ/OQ/PQ protocol execution against live systems. 83 automated test cases with cryptographic evidence collection. Signed, timestamped, verifiable reports ready for FDA inspection.
02
Pharma-Integrity Verified certification for CROs and contract manufacturers. Annual audit cycle. An industry-recognised standard that sponsors trust.
03
Audit preparation. Regulatory response. Gap analysis. Risk assessment. Former FDA expertise embedded in every engagement we deliver.
How it works
Your vendor installs their system in your environment. Standard infrastructure. Your data, your network, your controls.
We execute standardised qualification protocols against your live environment. Automated evidence collection. Cryptographically signed reports. Every test timestamped and traceable.
Your QA team reviews the generated report. Signs off. The system is qualified for regulated use. Inspection-ready from day one.