01 · Product definition
Approved formula, strength, dosage form, packaging specification, identification and shelf-life requirements form the controlled baseline.
Our approach connects product quality, GMP-certified controls, release governance, accessible information and post-market traceability.
Vertex Pharm combines pharmaceutical quality standards, GMP-certified manufacturing controls and market-specific product information in one traceable system.
Approved formula, strength, dosage form, packaging specification, identification and shelf-life requirements form the controlled baseline.
GMP-certified manufacturers, laboratories, materials and service providers are evaluated against documented requirements and ongoing performance.
Release is based on reviewed production, testing, deviation and specification records—not on marketing timelines.
Complaints, verification anomalies, safety information and changes feed back into the quality system.
Each valid combination of series and unique code is stored once. Every public check creates an audit record while personal network data is minimized through salted IP hashing.
Administrators can block or expire codes, associate them with products, import large code batches and review suspicious repeat activity.
Open product verificationImport series and unique codes from CSV, XLS or XLSX.
Link codes to a product, status and optional expiry date.
Check both values with rate limiting and atomic counters.
Review repeat, blocked, expired and unknown attempts.