Tracking software for the bench. Advisory support for the road to bedside.
Translational gaps are costly and come in many forms — a sample that lost its story, or an experimental design that never met regulatory standards. LIMS-SIN Tech addresses both: purpose-built sample tracking software, and advisory support from experimental design to regulatory submission.
Vial Tracker(s) Enabled by AI
The predecessor of Vial Tracker Free was built in 2004 in a NUS translational research lab (just like yours). The predecessor of Vial Tracker Cloud was built in 2014 with more advanced features in a translational research lab in a Singapore hospital and was used across multiple departments and institutes. No bug that caused a data issue was ever recorded.
With that track record, Vial Tracker Free and Vial Tracker Cloud were built from the ground up using AI-assisted development — not vibe coding. AI is woven into the product itself, not bolted on after. The heritage is 20 years old. The product is not.
We understand that staying bug-free and AI-powered is the floor, not the ceiling. In the regulated software world, the real hurdles are validation, audit trails, and change control — and we know exactly where they lie, so you won't have to find out the hard way.
Beyond IT and AI
Just like a sample that lost its story, a study designed without the regulatory endpoint in mind would stall or invalidate a translational program that took years to build.
Over the years, our team expanded the job scope to outside software development.
Our team's translational journey
Having sat on every side of the table, our value doesn't stop at software. If you're navigating the journey from translational research to bedside — whether that's sample tracking, data integrity, or the regulatory path ahead — we're happy to talk.
Questions, feedback, or just want to talk sample tracking?
Translational programmes don't begin with high-cost clinical research software — they begin at the bench, in Excel. But the responsibility to track sample lineage is exactly the same from experiment one. Vial Tracker Free gives any researcher a fully auditable record right where they already work, at no cost. No cloud account, no IT setup, nothing to install — and it works alongside whatever LIMS your institution already has.
From PostDoc departure to MTA compliance — explore use cases for your role:
You built your sample record with Vial Tracker Free — the lineage is documented, the discipline is there. Now your lab is taking on sponsored studies, clinical collaborators, or site audits. Vial Tracker Cloud picks up exactly where Free leaves off: multi-user, ALCOA+ compliant, and built to satisfy GCP, 21 CFR Part 11, and ISO 20387 — without the enterprise price tag or the IT overhead.
For labs that started right and are ready to grow. Whether you're graduating from Vial Tracker Free or stepping straight into the cloud tier — built-in role controls, timestamped records, and IQ/OQ documentation mean you enter your first audit compliant, not scrambling to become it.
Translational programmes run on documents as much as samples — SOPs, protocols, validation packages, regulatory submissions. MD-Review closes the AI-to-human-to-AI loop: your AI agent queues any markdown file for review, you read and comment inline exactly where the issue is, and the AI reads your feedback straight back — no copy-pasting, no lost context, no exported comment threads to reconcile.
A Windows app built for the AI era. Your AI drafts a document, hands it to MD-Review, and waits for your feedback — no copy-pasting files back and forth. Setup is one sentence: tell your AI agent to read the skill file and configure itself. Your documents and comments never leave your machine. Total privacy, by design.
Both products come with optional managed services. And if you need more than software — we've been on every side of the translational journey.
Begin with Vial Tracker Free — tracking sample lineage in Excel, at no cost, from experiment one. Graduate to Vial Tracker Cloud when sponsored studies, clinical collaborators, or site audits raise the stakes. LIMS-SIN Tech meets you at your stage — from bench tracking to IVD approval.