Restoring value to unused medicines,
with a compliant and traceable supply chain
ReVita Circle is the first European platform that enables pharmaceutical companies and distributors to redistribute unused batches in a compliant and verified manner to authorized healthcare facilities. More value, less waste, full compliance with GDP guidelines.
We reduce waste and disposal costs, enable a transparent supply chain and support access to essential medicines, without ever physically handling products.
Huge waste. Critical need. A gap we can close.
Every year millions of compliant pharmaceutical packages are disposed of due to lack of alternative channels, while in many areas of the world healthcare facilities lack access to essential medicines. ReVita Circle connects these two worlds in a compliant, verified and traceable way.
Surplus and disposal
Pharmaceutical companies and distributors produce excess batches to ensure supply continuity. However, in the absence of alternative channels and compliant digital solutions, many products end up incinerated with significant economic and environmental costs.
Unequal access to care
In many areas of the world, healthcare facilities and humanitarian organizations struggle to source basic medicines. This gap, aggravated by inefficiencies in global distribution, represents one of the main health challenges recognized by the WHO.
*Sources: AIFA, WHO (World Health Organization), OECD - estimates on pharmaceutical waste and access to essential medicines.
Technology and compliance at the service of global health
ReVita Circle is a B2B digital intermediation platform that facilitates the compliant redistribution of unused pharmaceutical batches, connecting companies and authorized healthcare facilities. We manage matching, verification, documentation and traceability digital intermediation, without direct product handling.
Security and compliance
We operate as digital intermediaries: KYB controls, licenses, VIES, verification of parties involved and end-to-end documentary traceability, without physical product handling.
Intelligent matching
Matching engine that cross-references active ingredient/ATC, country of origin/destination, import/export requirements, residual shelf-life, storage conditions and quantities, prioritizing urgent cases.
Network and global impact
Access to accredited healthcare organizations and logistics partners compliant with good distribution practices, for international redistributions in compliance with local regulations.
Dashboard & reporting
Operational and ESG KPIs: recovered batches, packages, residual shelf-life, avoided disposal costs and estimated CO₂. Exportable reports for audits and sustainability reports.
Verified partners
KYB onboarding with checks on VAT (VIES), licenses and documentation; references and post-transaction rating to ensure transparency and reliability.
Digital workflow
From registration to proof of delivery: batch publication, due diligence, match proposal, agreement, export/import documents, logistics and audit trail.
Ready to make a difference?
Talk to us: we verify requirements, use cases and compliant flows for your company.
5 steps towards concrete impact
A simple and compliant operational flow that digitalizes matching, verification, documentation and traceability digital intermediation, without direct product handling.
Registration and verification
Business onboarding with KYB checks: we verify identity, VAT (VIES), licenses and references. Automated document verification with human control for sensitive cases.
- KYB & VIES
- Licenses/authorizations
- Domain and references verification
Batch publication
Companies insert surplus with structured metadata for traceability: name, active ingredient/ATC, batch/lot and expiration, quantity, country of origin and storage conditions.
- Batch/lot and expiration
- Storage conditions
- Country of origin and quantity
Automatic matching
The matching engine cross-references supply and demand based on active ingredient/ATC, import/export requirements, residual shelf-life, temperature, volumes and operational priorities.
- Compliance criteria
- Expiration/urgency priority
- Logistics suggestions
Agreement and logistics
The parties finalize the agreement on the platform. Transport is carried out by certified logistics operators chosen by the parties; we provide documentary traceability, tracking and POD.
- Export/import documents
- Tracking and POD
- Cold chain where required
Impact and reporting
Dashboard with operational and ESG KPIs: recovered batches, packages, residual shelf-life, avoided disposal costs and estimated CO₂. Exportable reports for audits and sustainability reports.
- Live dashboard
- Exportable ESG reports
- End-to-end audit trail
Measurable impact, transparent methodology
ReVita Circle shows operational and ESG KPIs based on verified data: recovered batches, residual shelf-life, avoided disposal costs and estimated CO₂ through standard factors (GHG Protocol). Metrics become public when available and are accompanied by methodological notes.
Sources and method: WHO (Defined Daily Dose) for patient estimate; GHG Protocol for avoided CO₂; internal benchmarks and records for recovered batches. Metrics are published only after document verification.
Become a Founding Partner
Program dedicated to pharmaceutical companies and healthcare institutions who want to contribute to defining the new European standard for compliant pharmaceutical surplus redistribution.
- Priority access to the platform
- Involvement in the validation committee for standards and processes
- Personalized ESG reports and dedicated audit trail
- Early access to advanced features
- Preferential economic conditions
- Official "Founding Partner" badge