Service lines

Six specialist B2B channels, one regulatory backbone

Every channel runs through the same SOC2-audited documentation layer, the same licensed pharmacist review and the same GDP-grade shipping pipeline.

Named-Patient Procurement

Single-patient requests for therapies that aren't approved, commercially available, or temporarily out of stock in the requesting country — handled under named-patient import statutes with full paper trails.

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Contract Manufacturing Network

Tie-ups with WHO-GMP, US-FDA and EU-GMP inspected sites for generics, biologics and vaccines — with the audit reports attached, not promised.

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Clinical Trial Logistics

Comparator sourcing, rescue-medicine supply, co-medications and IMP movement with expiry-tracking, IRT integration and on-site reconciliation at investigator sites.

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Rare Disease Pathways

Orphan therapies routed through compassionate-use, named-patient and parallel-import pathways — for the 7,000+ conditions where local access doesn't exist.

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Institutional & Public Health Supply

Tender participation, direct procurement for ministries of health, NGO programmes and humanitarian supply corridors for high-burden disease therapies.

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Dossiers & Stability Programmes

CTD/eCTD compilation, ICH long-term and accelerated stability, and BA/BE analytics that get you across the table at the regulatory authority, not stuck outside.

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