Request feasibility ↗Donor recruitment, collection, component processing, testing, storage and traceable distribution in one controlled service.
Request feasibility study ↗Donor recruitment, collection, component processing, testing, storage and traceable distribution in one controlled service. The investment case is tested against import dependency, procurement demand, supply resilience, attainable local content and regional export access. Portfolio definition precedes equipment selection so capital is not locked into an incompatible process.
USD 1.2–6M. The range covers core equipment, controlled environments, process utilities, installation, qualification, technology transfer and initial training at the stated tier. Preliminary engineering range; excludes land, finance cost, taxes and import duty. Final scope and price are confirmed at the feasibility gate.
500–2,200 m² gross with segregated donor, processing, testing, quarantine, released storage and dispatch areas.
Blood banks generally use controlled hygienic zoning rather than classified cleanrooms. Component processing, testing and storage are separated with validated temperature and contamination controls.
8–14 months to operational qualification and supervised service launch. Permit, authority review, civil-condition, customs and client approval delays sit outside the base programme unless expressly contracted.
Tier 1: 20,000–60,000 donations/year; Tier 2: 100,000–250,000/year; operating days and collection network dependent.
Capacity assumes qualified materials, stated shifts, planned maintenance and validated yield; it is not the sum of nominal machine speeds.
Redundant power, UPS, emergency generation, temperature-mapped cold rooms/equipment, HVAC, secure data systems, infectious waste and validated transport.
National blood-service licence, donor/traceability rules and quality-system readiness; ISO 15189 may apply to testing laboratories. Typical readiness: 8–14 months.
Infinity IVD delivers the contracted facility, QMS, validation and dossier work. Certification or market authorisation is granted only by the competent independent authority.
Indicative 20–90 FTE including physicians, nurses/phlebotomists, laboratory scientists, quality and cold-chain personnel; 6–12 weeks systems and workflow training.
The feasibility equipment register identifies supplied equipment, client-supplied items, spares, initial consumables, FAT/SAT responsibility, calibration and qualification ownership.
Operating economics are issued as a sensitivity model using local labour, utilities, materials, yield, utilisation and financing assumptions; they are not a guaranteed return.
Client names and photography are disclosed only with permission; confidential programmes retain a technical envelope rather than an invented attribution.
Review programme evidence ↗The investor brief records the published assumptions, process flow, capacity tiers, regulatory route and data required for a binding feasibility package.