Artifacts VERIFY
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About
Artifacts VERIFY is a specialized solution designed to combat the global challenge of substandard and falsified (SF) drugs, which account for a significant portion of medicines in certain supply chains. By merging field-based chemical testing with advanced artificial intelligence, the platform provides a layer of security for healthcare providers, manufacturers, and regulators. Its primary goal is to identify ineffective or dangerous pharmaceuticals, particularly in regions where regulatory oversight may be limited, thereby aiming to reduce preventable deaths and preserve brand integrity within the medical industry. The system utilizes a multi-step verification process that begins with local testing using Paper Analytical Devices (PADs). Once a medicine is tested, the Artifacts AI engine interprets the chemical signatures to deliver initial findings. These results are then recorded on a secure blockchain to provide data integrity and traceability. The platform is capable of analyzing approximately 300 of the most commonly prescribed medicines, covering nearly 50% of the World Health Organization’s Essential Medicines list. It is designed to be deployed at any point in the supply chain, from initial manufacturing sites to the final point of care. This tool is intended for a range of stakeholders within the pharmaceutical ecosystem. Regulatory agencies can use it to monitor regional quality trends, while pharmacy managers and clinicians can check the authenticity of their stock before dispensing it to patients. Distributors and purchasers also utilize the platform’s reporting and analytics features, which highlight emerging hotspots where falsified drugs are appearing frequently. The inclusion of API access allows for integration into existing logistics and inventory management software, facilitating the tracking of lot numbers and manufacturer data. Unlike traditional laboratory testing which often requires significant time and cost, Artifacts VERIFY provides actionable intelligence directly via standard browsers and mobile devices. It fills a gap in existing safety monitoring by combining destructive local testing with centralized AI-driven analysis. The use of blockchain technology is intended to ensure that every test result is immutable and transparent, providing a standardized record of quality. This integrated approach to medicine quality surveillance offers a data-driven method for managing the risks associated with global pharmaceutical distribution.
Pros & Cons
Supports nearly half of the WHO Essential Medicines list.
Provides immediate AI interpretation of chemical test results.
Utilizes blockchain for immutable and transparent record-keeping.
Capable of identifying geographical hotspots for falsified drugs.
Can be deployed at any point in the supply chain via mobile devices.
Requires destructive testing of the medicine samples.
Currently limited to approximately 300 types of medicines.
Full chemical validation requires secondary laboratory confirmation.
Pricing information is not publicly available without a demo.
Use Cases
Pharmacy managers can verify the quality of incoming lot numbers to ensure patient safety before dispensing.
Regulatory agencies can track and visualize regional hotspots where falsified drugs are appearing frequently.
Pharmaceutical manufacturers can protect brand reputation by monitoring for counterfeit versions of their products.
Clinical trial coordinators can use the platform to confirm the integrity of medicines used during research studies.
Distributors can integrate the Verify API into logistics software to automate quality risk reporting.
Platform
Task
Features
• support for 300+ common medicines
• mobile and browser access
• lot number and manufacturer analytics
• api integration for reporting
• supply chain location tracking
• blockchain-backed results
• ai-driven initial findings
• chemical analysis interpretation
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. This includes nearly half of the W.H.O. Essential Medicines, and this coverage is expanded over time.
What data can Verify collect and report?
Verify collects essential information including location, protocol requirements, and results from chemical screens and assays. It also reports on the procedures and specific users engaged in handling medicines.
How does Verify identify the quality and safety of medicines?
Medicines are destructively tested locally with PADs and then interpreted by AI for immediate findings. To confirm safety, samples undergo further chemical analysis by certified laboratories.
What insight can be learned from the reporting and analytics?
Verify provides reports by lot number, manufacturer, and location to highlight hotspots where substandard drugs appear. It also identifies trends and predictive indicators of quality risks.
How are the test results secured and verified?
Scientifically validated results are recorded on a blockchain to ensure data integrity and transparency. This immutable record guides risk mitigation actions for purchasers, distributors, and regulators.
Pricing Plans
Custom
Unknown Price• Chemical analysis for 300+ medicines
• Real-time AI interpretation
• Blockchain data validation
• Supply chain hotspot reporting
• API access for integrations
• Mobile and browser compatibility
• Lot number tracking
• Historical trend analytics
Job Opportunities
There are currently no job postings for this AI tool.
Ratings & Reviews
No ratings available yet. Be the first to rate this tool!
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