Artifacts VERIFY
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About
Artifacts VERIFY offers a solution to combat the global problem of substandard and falsified medicines (SF medicines) in the pharmaceutical supply chain. By utilizing a combination of chemical analysis and artificial intelligence, the system allows for fast and effective testing of medicines, delivering initial findings in real-time. The scientifically validated results are recorded on a blockchain, ensuring risk mitigation actions are based on credible data. The tool can analyze approximately 300 commonly prescribed medicines, many of which are part of the W.H.O. Essential Medicines list, and provides extensive reporting and analytics on quality risks within supply chains.
Platform
Features
• comprehensive reports for risk mitigation
• scalable solution deployable at any supply chain point
• secure recording of results on blockchain
• ai interprets and reports findings quickly
• fast, effective testing of medicines
FAQs
How many medicines can be analyzed using the Verify system?
Approximately 300 of the most commonly prescribed medicines can be analyzed using the Verify system, which includes nearly half of the W.H.O. Essential Medicines.
What data can Verify collect and report?
Verify collects and reports essential information concerning medicines in the supply chain, including location, protocol requirements, primary data, and results from chemical screens.
How does Verify identify the quality and safety of medicines in the supply chain?
Medicines are destructively tested locally with PADs and undergo further chemical analysis by certified laboratories to confirm their safety.
What are the main benefits of using Verify?
Verify fills a critical gap in existing safety monitoring systems by providing actionable information from chemical analysis accessed from common browsers and mobile devices.
What insight and intelligence can be learned from the reporting and analytics available from Verify?
Verify provides reports of current and historical results by various factors, identifying trends and hotspots for substandard medicines.
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