TRSoftware and measurement systems that record every step of a critical biological product
We build the software that runs cellular therapy, biobanking and GMP manufacturing processes, the hardware that measures the environment they take place in, and the embedded systems that join the two — in one team. The institution buys one solution, and the record comes out ready for inspection.
The R&D company Labor İldam founded at Teknopark İstanbul
GoldenEye Solutions is the sister company that Labor İldam, active in laboratory and hospital equipment since 1979, established at Teknopark İstanbul in 2019 to carry its development work. Field experience on one side, R&D and manufacturing on the other; two faces of one business.
One party responsible for process, instrument and record
When process software, measurement hardware and field support come from three suppliers, responsibility scatters the moment something goes wrong. We develop all three under one roof.
Process, instrument and record under one roof
One team builds the software, the measurement instrument and the embedded firmware. When a temperature excursion happens, which samples were affected is a question the system answers.
Records built to the regulation
Structured to the expectations of 21 CFR Part 11, EU Annex 11, ISBT 128 and FACT-JACIE, and to tissue and cell regulation requiring thirty-year electronic retention.
A process defined per institution
Step count and data pattern differ by product in cellular therapy. Processes are defined with a drag-and-drop designer rather than fixed in code.
Support that stays in the field
Annual maintenance and support after installation, remote access, and on-site intervention through the Labor İldam service network across Turkey.
Software that runs the process, hardware that measures the environment
BIOSECURE modules are licensed to the institution's requirement; measurement and monitoring instruments work with our own software and with existing systems.
BIOSECURE
A single platform for cell and tissue manufacturing, biobanking, transplant and cord blood processes — from patient and donor registration through processing…
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GE-MON
Central monitoring and alarm management for critical equipment and environments: ULT freezers, cryogenic tanks, incubators, cleanrooms and infrastructure, with…
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GE-100 MultiSensor
A single unit measuring oxygen, carbon dioxide, differential pressure, temperature and humidity, with local visual and audible alarms and relay outputs for…
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GE-202
IoT module for temperature, humidity and alarm contact monitoring, with WiFi, Ethernet and RS485, MQTT and Modbus support, and local buffering when the network…
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GE-EDGE
An edge gateway that collects data from equipment of different makes and protocols, pre-processes it locally and delivers it securely over MQTT, Modbus and OPC…
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GE-SCAN
Reads all coded vials in a cryogenic box in a single capture inside a closed enclosure and reconciles them against the expected layout in the sample database.
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CryoCap
Level and temperature monitoring for cryogenic tanks, designed to be retrofitted to tanks already in service.
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Cryogenic automation
Automatic liquid nitrogen filling, cylinder changeover and vacuum-jacketed line design, with oxygen safety interlocks and central monitoring.
Read more →Configured to the work your institution does
The same product family is configured differently in a transplant unit, a biobank, a GMP manufacturing facility and an IVF laboratory.
Installations running in the field
Systems installed at more than 35 institutions, including transplant centers, biobanks, GMP manufacturing facilities and research laboratories.
Institution names and logos are published only with written permission. Reference list →
The record is no longer optional. It is a condition of operating
Across jurisdictions the requirement has converged: an establishment must operate a traceability system, label to a recognized coding standard, and retain records electronically for decades after clinical use, with unauthorized addition, deletion and modification prevented.
- Procurement, processing, storage, distribution and clinical use records in one system
- ISBT 128 coding and FACT-JACIE 9.1 expectations
- Audit trail and electronic signature per 21 CFR Part 11 and EU Annex 11
- Maintenance, calibration and business continuity records for critical equipment
We manufacture our boards at our own facility at Teknopark İstanbul
The surface-mount line we built in 2026 with KOSGEB SME technology investment support comprises a placement machine, reflow oven, conveyor, and test and soldering stations.
- Variant production: The same upper board becomes a different measurement set with a different lower board; production for a single institution is viable.
- Spare part continuity: The board in a field instrument can still be manufactured years later.
- Short development cycle: Design, prototype and field test happen in the same building.
- Local manufacturing: A faulty board is not shipped abroad; lead time comes down to weeks.
What we have written on standards, regulation and field practice
Twenty technical and clinical articles, each grounded in international guidance and field practice.
Let us talk about your processes
Share your process steps and equipment list; we will work out scope, deployment and schedule together.