VeriPura Pharma™ is VeriPura Core tuned for pharmaceuticals. Agents trained on import licensing, good manufacturing and distribution practice, serialization and registration rules check every document against the requirements of any country of origin and any country of destination before the shipment moves, not at the border. Each shipment gets findings, the fixes it needs, and a record anyone can verify. Engage it from your own systems, or have us run the checks for you.
Built on VeriPura Core™ and its 50+ specialist agents. Tuned to your products, routes and documents.
Hyderabad, India to Antwerp, Belgium
Substandard and falsified products enter supply chains through gaps in documents and checks. Every import needs the right licences, certificates and records, and they must match each other and the product.
VeriPura Pharma™ runs the same find, check and prove loop as every industry solution built on VeriPura Core™. For pharmaceuticals, the agents are tuned on import licensing, good manufacturing and distribution practice, active substance rules, serialization and product registration, and the authorities and bodies that certify them. At the check stage, agents do not rely on the documents alone: they take in inputs from third-party validators and cross-check claims against independent data sources, so each finding rests on an outside source of truth, not only on what the paperwork says.
Work out what applies.
Test every document field against the rules, third-party validators and independent data sources.
Leave a verifiable record.
Keep your ERP and your interface. VeriPura Pharma provides rules, tuned agents and an evidence trail through our hosted API.
// tool call from your own system
check_compliance({
hs_code: "2941.10",
origin: "IN",
destination: { country: "BE" },
documents: ["coa.pdf", "gmp_cert.pdf", "written_confirmation.pdf"]
})
// response
{
status: "review",
findings: [{
check: "written_confirmation",
result: "mismatch",
detail: "manufacturing site differs from GMP certificate",
source: "independent_registry",
confidence: 0.96
}],
evidence_id: "vp:folder:PH-7731",
anchored: true
}Tuned for pharmaceuticals, VeriPura Core can check any pharmaceutical product moving from any origin to any destination, wherever the rules can be obtained. The rules below are examples only.
For example marketing authorisations, import licences and US drug establishment registration.
For example EU GMP and GDP, written confirmations for active substances, and WHO prequalification.
For example the EU Falsified Medicines Directive and the US Drug Supply Chain Security Act.
For example import and export authorisations for controlled substances, and temperature records.
The product, its origin and destination, and any certifications your customers require beyond import regulations.
The agents identify the HS code, the rules that apply and every document the shipment needs.
The agents are trained and tested on sample documents for that route, then put to work on it.
Examples of tools that can be built on the pharma-tuned agents. They are not yet available. Tell us which would help your team, or call the agents directly from your own systems.
Confirm a certificate against the issuing authority's public records.
Example. Not yet available.Check that licences, certificates and the batch record match each other and the product.
Example. Not yet available.Validate product identifiers and traceability data against the destination's requirements.
Example. Not yet available.The same options as every industry solution built on VeriPura Core, priced per transaction checked.
For manufacturers, importers and distributors with a specific problem
For teams that want the outcome, not the build
When a shipment is rejected, the importer looks to the forwarder first. VeriPura turns that liability into a service and a revenue stream.
VeriPura Core tuned for pharmaceuticals. It checks licences, GMP and GDP certificates, certificates of analysis, batch records and cold chain data against the requirements of any country of origin and any country of destination before a shipment departs.
VeriPura Pharma™ is the industry solution built on VeriPura Core™ tuned for pharmaceuticals: the same orchestrated agent engine, with agents trained on pharmaceuticals rules, documents and certifiers. Other industries, such as food, cosmetics and supplements, have their own tuned editions.
Yes. The orchestration and verification approach is covered under VeriPura's USPTO filing, U.S. provisional patent application 64/088,697. The filing secures our date for later non-provisional and foreign patent filings.
Yes, through our hosted API. Talk to an engineer to discuss what your team needs.
Certificates of analysis, GMP and GDP certificates, written confirmations, import licences, marketing authorisations, batch records, temperature logs, controlled substance permits and the other documents the destination market requires.
Any framework for any country of origin and any country of destination, wherever the rules can be obtained. Examples include EU Directive 2001/83/EC and the Falsified Medicines Directive, EU GMP and GDP, the US Drug Supply Chain Security Act and FDA import requirements, and WHO guidelines.
Agents compare each document with the others and with independent sources, such as public registers of manufacturing sites, and flag mismatches that could point to a substandard or falsified product before the shipment moves.
No. It prepares the evidence and flags issues. Your qualified people make the decisions.
It starts with one real shipment. We show every rule that applied, what was missing and any red flags. Your team makes the decision. If it's useful, a paid pilot follows in shadow mode, with the fee credited toward a contract.
Send us the documents for one real shipment and we'll show you every rule that applied, what was missing and any red flags. If it's useful, the next step is a paid pilot in shadow mode, with the fee credited toward a contract.
18+ years in import and export compliance across Southeast Asia and Europe.
Serial entrepreneur and patent holder with a background in B2B go-to-market.
35+ years in enterprise solutions architecture, including SAP delivery, and a decade building blockchain products for real-world use cases.