Category Archives: 2026

How a LIMS Improves Quality Control in Manufacturing Laboratories

How a LIMS Improves Quality Control in Manufacturing Laboratories

Imagine that a batch is ready to leave the warehouse, waiting on one thing which is lab sign-off on a Friday. Somewhere between a spreadsheet, an inbox and a paper form is the result confirming the product can ship. This isn’t a rare event for manufacturing labs, it’s an everyday consequence of manual quality control.

According to industry research, laboratory staff can spend a significant portion of their day on admin tasks such as manually entering data, searching for records and preparing documentation instead of performing analytical work. Sometimes a compliance officer digs through binders before an audit, hoping nothing’s missing. Sometimes a supervisor manually re-keys the numbers into a report for the plant manager. None of this is because the people running these labs aren’t good at their jobs. It’s because the tools they’re working with were never built for the volume, complexity, or speed manufacturing demands today.  This is where a question comes to mind: Why does LIMS matter for manufacturing LIMS

Why LIMS matters and why now

A Laboratory Information Management System (LIMS), exists to take the manual grind out of running a lab: sample tracking, testing workflows, results, compliance records, all in one connected system instead of scattered across paper, inboxes, and spreadsheets.

While production lines have embraced automation, laboratory data is often still managed using paper, spreadsheets and disconnected systems. That gap is becoming harder to ignore.

The labs still relying on paper and spreadsheets aren’t just slower — they’re carrying risk every single shift.

That’s the moment LIMS steps onto the stage: not as a nice-to-have digitisation project, but as the system that lets a manufacturing lab keep pace with the plant around it. (If you’d like to read what a LIMS is, click here.)

 

How a LIMS actually improves quality control

A modern LIMS changes QC on the floor in a few concrete ways:

  • Faster sample turnaround. Digital sample booking and automated routing mean a sample gets logged, assigned, and tracked the moment it hits the lab.
  • Fewer manual errors. Manual data entry creates unnecessary risk. By connecting directly with instruments and capturing results electronically, a LIMS reduces transcription errors, eliminates duplicate entry, and ensures data is linked to the correct sample every time. 
  • Risk-based testing. Not every product or batch requires the same level of testing. A configurable LIMS can apply predefined rules based on product type, risk level, or testing requirements, helping laboratories focus resources where they matter most while maintaining quality standards. 
  • Audit-ready by default. Every sample, test, and result is logged automatically with a full chain of custody, so an audit becomes a report you pull, whenever it is needed. 
  • Real-time visibility. Production leaders and quality leads can see batch status without pinging the lab, so “is it ready to ship?” gets an instant answer instead of a phone call.

Put together, these aren’t just efficiency gains. They’re the difference between QC being a bottleneck and QC being a competitive advantage.

This is where QLIMS comes in

QLIMS is built specifically for labs like these, manufacturing QC labs that need to move fast without losing rigor. It replaces paper forms and Excel trackers with digital sample booking, automated workflows, and no-code configuration, so labs can adapt the system to their processes instead of bending their processes to fit rigid software.

No two manufacturing labs test the same way, and QLIMS is designed around that reality: configurable testing protocols, automated risk-based rules, and reporting that’s ready for an auditor the moment it’s requested. The goal isn’t to add another system on top of the chaos, it’s to remove the chaos underneath the work labs are already doing.

Real labs, real results

Not all LIMS vendors claiming to support precision medicine actually do. Here is what separates platforms that deliver from those that overpromise.

The proof isn’t in the pitch. It’s what happens when manufacturers actually put a LIMS to work.

  • Baiada replaced manual, paper-based sample submissions with QLIMS and freed up 1.5 full-time-equivalent roles that had been consumed by chasing forms and re-entering data. That’s not a marginal saving; that’s over a full headcount redirected toward work that actually needs a human.
  • Comvita moved its technicians off manual Excel spreadsheets and onto QLIMS, and saw a 20% jump in technician efficiency. Same team, same skills, but  just far less time lost to spreadsheet admin.
  • A confectionery manufacturer used QLIMS to automate risk-based testing protocols, cutting down the number of tests run on lower-risk products without compromising on the ones that matter. Less redundant testing, same confidence in the result.

Three different industries. Three different problems. The same underlying story: when the manual work disappears, the lab gets faster, the results get more reliable, and the people running it get their time back.

Every manufacturing laboratory reaches a point where paper forms, spreadsheets and disconnected systems begin to limit performance rather than support it. A modern LIMS helps laboratories spend less time managing information and more time delivering accurate, timely quality results.

If your lab is still running on paper and spreadsheets, the question isn’t whether a LIMS would help. It’s time to evaluate whether your current processes are still keeping pace with your operation. Book a demo with us today to see firsthand how we could support you. 

What Is a LIMS for Precision Medicine — And Why Most Labs Get It Wrong

OnQ Software - LIMS For Precision Medicine

Precision medicine is rewriting the rules of diagnostics. Genomic sequencing, targeted oncology, and molecular pathology are no longer niche capabilities. They are the new baseline for forward-thinking labs. But the infrastructure holding these labs together? That is often still stuck in the past.

Most laboratory information management systems were designed for routine sample tracking, not the complex, multi-stage workflows that precision medicine demands. The result is labs running world-class science on outdated software, patching the gaps with spreadsheets, manual workarounds, and disconnected tools.

A LIMS for precision medicine is not just a standard LIMS, it is a fundamentally different type of platform, which is the one built for the data complexity, regulatory rigour, and clinical accountability that precision medicine requires.

What sets a precision medicine LIMS apart

A standard LIMS handles sample accessioning, result entry, and basic reporting. That is table stakes. Precision medicine workflows go further, a single patient specimen can generate genomic, transcriptomic, and proteomic data across multiple instruments and analytical stages. The system managing that journey needs to do more.

A LIMS for precision medicine labs should handle:

  • Automated import of molecular data, including NGS instrument integration and automated sample sheet generation
  • End-to-end traceability, from sample receipt through nucleic acid extraction, library prep, sequencing, and clinical reporting
  • Stage gate workflows that enforce quality control at every step, preventing errors from progressing downstream
  • Built-in compliance with ISO 17025 and ISO 15189 standards, including complete audit trails for sample handling
  • Clinical modules for patient and physician tracking, with secure report distribution and real-time delivery notifications
  • HL7 support for direct integration with hospital information systems and electronic health records

Without these capabilities, labs are forced to bridge the gaps manually which introduces exactly the kind of human error that precision diagnostics cannot afford.

The compliance challenge most labs underestimate

Regulatory compliance in precision medicine is not just about passing an audit. It is about building a system where trust in data is built into every process by default.

In high-stakes environments — oncology diagnostics, genetic testing, molecular pathology — the consequences of a documentation failure are not just operational. They are clinical. A sample without an unbroken chain of custody, a result without a time-stamped record, a report delivered to the wrong physician: these are not edge cases. They are risks that need to be designed out.

Paper-based systems and general-purpose LIMS platforms cannot reliably support this level of accountability. Electronic records need to be time-stamped, version-controlled, and immutable. Workflows need to enforce process integrity, not just record that a step was completed, but prevent the next step from proceeding until compliance criteria are met.

LIMS for precision medicine in the real world: a Bangladesh case study

One of the most compelling demonstrations of what a precision medicine LIMS can achieve comes not from a well-resourced first-world hospital, but from a molecular pathology lab being built in Bangladesh.

An oncology and nanotechnology research organisation engaged QLIMS to support the delivery of rapid point-of-care cancer diagnostics and genetic testing in one of the world’s Least Developed Countries (LDCs). The challenge was significant: limited regulatory infrastructure, language and cultural barriers across the lab team, and the need to meet international quality standards from day one.

The organisation evaluated four LIMS platforms. QLIMS was selected for its no-code configurability, multilingual visual interface, and high-security architecture, capabilities that mattered as much in Bangladesh as they would in London or Sydney.

The deployment included:

  • Automated Illumina sequencing integration with sample sheet generation and mutation identification
  • Centralised data management across results, instrument logs, and reagent records
  • ISO 17025 and ISO 15189-compliant audit trails from day one
  • Secure clinical report distribution with real-time SMS tracking for physicians

Data lake infrastructure to capture population-level genomic data unique to South Asian genetic profiles, not typically represented in Western datasets

The outcome: a lab now delivering world-class oncology diagnostics in a region that previously had no such capability. External auditors described QLIMS as one of the most sophisticated and easy-to-use systems they had ever assessed.

The broader impact is significant. Bangladesh spends an estimated USD 5 billion annually on citizens seeking medical treatment abroad. By raising the standard of diagnostic capability domestically, the country can begin to recapture those patients and provide equitable access to precision medicine for populations historically excluded from it.

What to look for when evaluating LIMS for a precision medicine lab

Not all LIMS vendors claiming to support precision medicine actually do. Here is what separates platforms that deliver from those that overpromise.

No-code configuration

Precision medicine workflows evolve quickly. If adapting your LIMS to a new assay or regulatory change requires a software developer, you are already behind. Look for a platform that allows lab managers and informatics teams to configure workflows, fields, and reports without code.

Instrument integration

Manual data entry between instruments and your LIMS is a reliability risk. LIMS should integrate directly with your sequencing and analytical platforms, automating data import and eliminating transcription errors.

Scalability and AI readiness

The labs winning in precision medicine are the ones building data infrastructure now that will support AI-powered analysis later. Look for a LIMS that supports data lake architecture, structured data capture, and a clear roadmap for AI integration. 

Compliance by design

Regulatory compliance should be built into the platform, not bolted on. ISO-compliant audit trails, stage gate workflow controls, and document version management should come standard, not as premium tiers.

QLIMS: precision medicine LIMS built for modern labs

QLIMS is a SaaS LIMS designed specifically for the complexity of precision medicine, genomics, and molecular diagnostics. It brings automation, instrument integration, and clinical reporting into a single secure platform without requiring IT infrastructure or software developers to configure and maintain it.

Used by genomics and oncology labs across globally, QLIMS is built for labs that operate at the frontier of medicine where the stakes are high, the data is complex, and the infrastructure needs to be as advanced as the science.

If you are evaluating LIMS platforms for a precision medicine or genomics lab, we would be happy to show you what QLIMS can do.

Book a Demo Here. Read the Bangladesh Case Study Here

When Does a Laboratory Need a LIMS? 7 Signs You’ve Outgrown Spreadsheets

when does a laboratory needs LIMS

When does a laboratory need a LIMS? It’s one of the most common questions laboratory managers ask as their operations grow. Spreadsheets are where everything begins. A few samples become a few hundred. A simple tracking sheet becomes several workbooks. Then more tabs are added, formulas become more complex, and suddenly the entire laboratory is relying on a system that was never designed to manage laboratory operations.

The spreadsheet that solved yesterday’s problem could be creating tomorrow’s bottleneck.

At first, spreadsheets feel flexible and familiar. But as workloads grow, compliance requirements increase, and teams expand, they can quietly become one of the biggest barriers to efficiency.

So how do you know when your laboratory has outgrown spreadsheets?

Here are seven common signs:

1. Your Team Is Spending More Time Managing Data Than Performing Science

Scientists, technicians, and quality teams should be focused on testing, analysis, and decision-making.

Instead, many laboratories find themselves manually entering results, updating multiple files, copying data between systems, and checking formulas.

The result? Valuable time is spent maintaining records rather than generating insights.

For example, entering 100 sample results may only take a few minutes. But repeat that process multiple times per day, across multiple analysts, and those minutes quickly become hours every week.

A LIMS automates much of this administration, allowing teams to focus on higher-value work.

2. Sample Tracking Is Becoming Difficult

One of the earliest warning signs is losing visibility of sample status.

Questions such as:

  • Has this sample been tested?
  • Who approved the result?
  • Which version of the report is correct?
  • Where is the sample now?

often become more frequent as volumes increase.

A laboratory processing 20 samples per day may manage comfortably using spreadsheets. A laboratory processing 200 samples per day often struggles to maintain visibility without a centralised system.

A LIMS provides real-time tracking from sample receipt through to reporting.

3. Audit Preparation Feels Stressful

Audits should not require days of searching through folders, emails, and spreadsheets. If your team spends significant time gathering evidence, proving traceability, or reconstructing records, your current process may be creating unnecessary risk.

Modern laboratories increasingly need:

  • Complete audit trails
  • User accountability
  • Electronic approvals
  • Controlled data access

These requirements are difficult to manage consistently using spreadsheets alone.

4. Errors Are Becoming More Common

Spreadsheets are powerful tools, but they are also highly dependent on human input.

A single accidental formula change, duplicate entry, or copy-paste mistake can impact reporting, investigations, and compliance.

As laboratory complexity grows, the likelihood and cost of these errors grows with it.

Consider a laboratory generating hundreds of reports per month. Even a small error rate can lead to significant rework, delayed reporting, or customer dissatisfaction.

As laboratories grow, reducing human error becomes increasingly important.

5. Different Teams Are Working in Different Systems

Many laboratories find themselves storing information in several locations:

  • Sample tracking in spreadsheets
  • Results in shared folders
  • Quality records in separate systems
  • Instrument data stored independently

For example, generating a single client report may require information from three or four different sources. This creates data silos.The more disconnected the data, the harder it becomes to maintain efficiency and confidence in decision-making.

A LIMS creates a single source of truth, bringing data, workflows, and reporting together in one platform.

6. Growth Is Creating Operational Pressure

Growth is often the point where spreadsheets begin to struggle.

Perhaps your laboratory has:

  • Added new testing methods
  • Expanded into multiple locations
  • Increased sample volumes
  • Hired additional analysts
  • Won larger customer contracts

What worked for a small laboratory rarely scales efficiently.

If every increase in workload requires additional manual administration, your systems may be limiting future growth.

A modern LIMS helps laboratories scale without increasing complexity at the same rate. Scalable laboratories need scalable systems.

7. Reporting Takes Longer Than It Should

Laboratory data is valuable only when it can be accessed, reviewed, and shared efficiently.

If teams are spending hours compiling reports, validating data, and manually creating customer deliverables, reporting may have become a bottleneck.

A modern laboratory informatics platform can help streamline reporting by keeping data connected from sample receipt through to final approval. You can simply click on the “Generate a CoA” in a modern LIMS and automate your report process. 

A Simple Rule of Thumb 

There is no perfect time to implement a LIMS. However, laboratories should begin evaluating their options if they:

  • Conduct more than 500 tests per month
  • Have multiple staff entering or reviewing results
  • Need stronger compliance and traceability
  • Struggle to track samples efficiently
  • Spend significant time preparing reports or audits
  • Plan to grow over the next few years

The best time to implement a LIMS is often before operational challenges become business problems.

Ready to See What a Modern Laboratory Platform Looks Like?

QLIMS helps laboratories centralise sample management, automate workflows, strengthen compliance, and reduce manual administration within a configurable cloud-based platform.

Whether you’re managing hundreds of samples or hundreds of thousands, QLIMS is designed to grow with your laboratory.

Book a personalised QLIMS demonstration and discover how modern laboratories are replacing spreadsheets with connected, scalable laboratory informatics.

Press Release: QLIMS Expands Across the Gulf and Jordan Genomics Market Through Strategic Partnership with Legion BioSolutions

OnQ Software - LIMS For Precision Medicine

Melbourne, Australia – June 4, 2026:

Legion BioSolutions Limited and OnQ Software Pty Ltd are pleased to announce that they have signed a dealer agreement appointing Legion BioSolutions as the regional partner for QLIMS, OnQ Software’s flagship laboratory information management system, across the genomics sector in the United Arab Emirates, Saudi Arabia, Bahrain, Kuwait, Oman, Qatar, and Jordan.

Under the agreement, Legion BioSolutions will lead promotion, distribution, configuration, and regional support for QLIMS deployments to genomics laboratories, research institutions, and national programmes across the territory. This expands Legion BioSolutions’ professional services offering with a mature, cloud-native LIMS platform purpose-built for high-throughput, regulated environments, directly addressing one of the most pressing infrastructure needs reported by the institutions Legion is currently engaged with.

QLIMS is a modern SaaS laboratory informatics platform trusted by laboratories worldwide, with a strong track record in genomics including major institutions such as Children’s Cancer Institute Australia. The platform offers no-code configuration, API-driven integrations, and an evolutionary architecture that allows laboratories to adapt as their needs change, alongside built-in support for industry standards including ISO 17025 and FDA 21 CFR Part 11. QLIMS can be integrated with Illumina, Oxford Nanopore and MGI sequencing devices allowing seamless experimental tracking. Recent releases have introduced advanced project management, instrument tracking, in built business intelligence dashboards, and the QLIMS Bridge Module for instrument and data system integration.

For OnQ Software, the partnership provides specialist regional reach into a market where demand for clinical-grade, scalable LIMS infrastructure is accelerating. Legion BioSolutions brings deep technical and commercial relationships across the region’s genome programmes, research hospitals, and precision medicine initiatives, along with the bioinformatics and data engineering expertise to ensure QLIMS implementations integrate cleanly into broader sequencing and analytical workflows.

The agreement forms part of Legion BioSolutions’ broader strategy to assemble a best-in-class, vendor-agnostic technology stack for the institutions building the next generation of genomic infrastructure across the Middle East, combining specialist analytical, sample management, and data governance tools under a single regional point of contact.

“Sample tracking, workflow management, and audit-grade data governance are foundational to every credible clinical genomics programme – and the institutions we work with in the Gulf are building these capabilities at pace. OnQ Software has built a LIMS platform that is genuinely modern: cloud-native, no-code configurable, and proven in genomics environments. We’re proud to bring QLIMS to our clients as the LIMS layer of choice for the region’s most ambitious programmes.”

Dr Bhupinder Hundle, Co-Founder & CEO, Legion BioSolutions

“We are incredibly excited to partner with Legion BioSolutions to introduce QLIMS into the crucial genomics markets of the Gulf and Jordan. The region’s commitment to building world class national genome programmes requires robust, scalable, and modern informatics infrastructure. Legion BioSolutions’ deep local expertise and technical strength in bioinformatics make them the ideal partner to ensure QLIMS, a platform proven in high-throughput genomics, integrates seamlessly and supports these ambitious, clinical grade initiatives.”

Jonathan Gannoulis, CEO, OnQ Software


About OnQ Software

OnQ Software is at the forefront of laboratory informatics, helping laboratories modernise operations, improve data integrity, and accelerate scientific outcomes through advanced digital solutions.

QLIMS is a lab grown modern, scalable and affordable Laboratory Information Management System (LIMS) that serves as a comprehensive platform for laboratory data management and workflow automation, particularly in genomics and sequencing environments. 

For more information, visit onqsoft.com

OnQ Software ǀ 6, 405 High Street, Northcote, Melbourne VIC Australia ǀ Phone  +61 3 8582 6999 ǀ info@onqsoft.com

About Legion BioSolutions

Legion BioSolutions Limited is a UK-based life sciences technology and professional advisory company specialising in bioinformatics, data engineering, and informatics software for genomics and proteomics. The team provides data and pipeline architecture, variant workflows, custom databases, LIMS integration, scalable compute environments, tech selection, machine learning analytics, and regulatory data management. Founded by experienced Oxford Nanopore alumni with strong genomics and protein science backgrounds, Legion BioSolutions collaborates with global precision medicine initiatives, genome councils, and research hospitals to deliver expert data solutions at clinical and high-throughput scale.

For more information, visit legionbiosolutions.com

info@legionbiosolutions.com


Press Contacts

OnQ Software
Email: info@onqsoft.com
Phone: +61 3 8582 6999

 

As Public IVF Expands, Digital Transformation Matters More Than Ever

Public IVF Expands, Digital Transformation Matters More Than Ever

For many families, IVF represents hope. Hope for a future they have dreamed about for years. Hope after difficult diagnoses, long waiting periods, and emotional uncertainty. As access to fertility treatment expands globally, more people are now gaining access to services that were previously financially out of reach.

Across countries such as Australia, the United Kingdom, Canada, and parts of Europe, governments are increasingly expanding or subsidising fertility treatment, reflecting a broader shift toward making IVF more accessible through public healthcare systems. Recently, the Victorian Government announced a $43.4 million expansion of publicly funded IVF services, aiming to make fertility care more accessible for Victorians (Victorian Government, 2026). This marks an important step forward for healthcare accessibility and reproductive medicine.

But behind every fertility journey is something often overlooked: the laboratory.

Modern IVF and fertility laboratories manage incredibly complex workflows every single day. From sample tracking and embryo monitoring to patient data, compliance documentation, reporting, and genetic testing, these environments generate vast amounts of highly sensitive information. As public IVF services grow, so does the operational pressure placed on laboratories. More patients mean more data, more workflows and greater expectations around accuracy and turnaround times. And of course, in fertility care, precision matters.

Even small administrative or data handling errors can have significant consequences. That is why digital transformation is becoming increasingly important across IVF and reproductive medicine.

The Shift from Manual Processes to Connected Digital Ecosystems

Many IVF laboratories still rely on fragmented systems, spreadsheets, paper-based workflows, or disconnected software platforms. While these processes may have worked in the past, they become increasingly difficult to manage as demand grows.

IVF laboratories require seamless coordination between:

  • clinicians
  • embryologists
  • genetic testing workflows
  • laboratory instruments
  • patient records
  • reporting systems
  • compliance documentation

Without connected systems, laboratories can face workflow bottlenecks, duplicated administrative work, reduced visibility, and increased risk of human error. Digital laboratory platforms help solve these challenges by centralising information, automating workflows, and improving traceability across the entire laboratory ecosystem. Instead of spending valuable time managing administrative complexity, laboratory teams can focus more on patient care and scientific outcomes.

Why Traceability and Data Integrity Matter in IVF

OnQ Software - LIMS For Precision MedicineIn fertility laboratories, traceability is not simply an operational benefit, it is critical. Every sample, every workflow stage, and every data point must be accurately tracked and documented. Laboratories must maintain strict compliance standards while ensuring transparency and accountability throughout the entire process.

Modern laboratory informatics platforms help support this through:

  • audit trails
  • workflow automation
  • secure data management
  • automated reporting
  • controlled user access
  • instrument connectivity

These capabilities not only improve operational efficiency but also help laboratories build trust, consistency, and long-term scalability.

How Agentic AI Transforms IVF Laboratories

Unlike traditional automation, which follows fixed rules, agentic AI systems are designed to understand context, interpret questions, and take action across connected systems. In a fertility or genomics environment, this means laboratory teams are no longer limited to manually searching across systems, dashboards, or documents to find answers or trigger workflows.

Instead, they can simply ask questions in natural language and receive operationally meaningful responses.

For example:

  • Which patient samples are currently in fertilisation or monitoring stages?
  • Which instruments are currently in use or available?
  • What embryo culture workflows are scheduled for today?

These are not just “information queries.” They are operational decisions that usually require navigating multiple systems, checking availability, reviewing workflows, and cross-referencing data. Agentic AI has the potential to bring this together into a single intelligent layer across the laboratory.

Recent research in reproductive medicine and biomedical AI supports this direction, highlighting that the integration of AI into clinical and laboratory environments is increasingly focused on improving decision support, workflow efficiency, and data-driven coordination rather than simply automating isolated tasks. In particular, studies such as those published in Biology (MDPI) emphasise the growing role of AI in consolidating complex reproductive datasets and enabling more context-aware interpretation of embryology and clinical workflows, reinforcing the shift toward integrated, intelligence-assisted laboratory systems (Hew, Y., Kutuk, D., Duzcu, T., Ergun, Y., & Basar, M. (2024). Artificial intelligence in IVF laboratories: elevating outcomes through precision and efficiency. Biology13(12), 988.).

In IVF environments specifically, this becomes even more powerful.

Imagine a system that can understand embryo culture workflows, patient timelines, sample status, and instrument availability in real time, and then proactively assist laboratory staff in coordinating the next best action. Instead of teams manually tracking where each sample is or which step comes next, AI could surface bottlenecks, suggest prioritisation, or even trigger actions within defined governance rules.

This is where platforms like Sophia AI, built into modern laboratory ecosystems such as QLIMS, are starting to redefine what “laboratory informatics platforms” actually means.

Rather than being passive systems that store and organise data, they begin to behave more like active collaborators inside the lab. Systems that don’t just record what happened, but help decide what should happen next.

In IVF and reproductive medicine, where timing, sequencing, and precision are critical, this shift can have a meaningful impact. Faster access to answers, fewer manual handovers between teams, and reduced cognitive load on embryologists and laboratory managers all contribute to more efficient and more resilient operations.

Over time, the role of laboratory staff may shift less toward searching for information and more toward supervising intelligent systems that handle routine coordination in the background, while still keeping humans in control of clinical and scientific decisions. This is not about replacing expertise, it is about amplifying it.

As IVF laboratories continue to evolve, the real impact of these technologies is best understood when seen in practice. Reading about connected systems and agentic AI only goes so far; the real value becomes clear when you experience how they interact with everyday lab workflows. If you’d like to see how Sophia AI can answer real IVF laboratory questions and support day-to-day decision-making in action, feel free to get in touch with us. We’d be happy to walk you through it and show what it looks like in a real lab environment.

Press Release: QLIMS joins the Oxford Nanopore Compatible Products Programme

QLIMS joins the Oxford Nanopore Compatible Products Programme

Melbourne, Australia – May 19, 2026:

QLIMS is a lab-grown cloud laboratory information management system (LIMS), announced that they have joined the Oxford Nanopore Technologies Compatible Products Programme, a global ecosystem of validated solutions designed to support nanopore sequencing workflows. 

As genomics laboratories continue to scale sequencing operations, they face increasing complexity in managing samples, sequencing data, and downstream analysis across multiple systems. This fragmentation can slow workflows, increase manual effort, and limit the ability to scale efficiently.

QLIMS addresses these challenges by providing a cloud-based, end-to-end platform for sample tracking, sequencing data management, and reporting. Built for genomics and Oxford Nanopore sequencing workflows, QLIMS helps laboratories reduce manual processes, improve data traceability, and support both wet lab and dry lab operations within a single system. The platform also includes AI-powered tools to enhance efficiency across experimental and analytical workflows.

“Joining the Compatible Products Programme is an important milestone for us,” said Jonathan Gannoulis, CEO of OnQ Software. “It reflects our commitment to supporting modern genomics laboratories with connected, scalable solutions that bring structure to increasingly complex sequencing workflows.”

Through its Compatible Products Programme, Oxford Nanopore works with innovative organisations to verify third-party products for use with its platforms. The compatible product ecosystem brings together trusted assays, data management and analysis solutions, and automation platforms that empower users to diversify, streamline and scale workflows on their Oxford Nanopore platforms. By joining this ecosystem, QLIMS strengthens its position as a flexible informatics layer that supports seamless data and workflow management in nanopore sequencing-based environments.

This development supports a wide range of genomics applications, including translational and clinical research, and biotechnology, enabling organisations to focus on what truly matters: advancing science and delivering real-world impact. 

 

About OnQ Software

OnQ Software is at the forefront of laboratory informatics, offering cutting-edge solutions designed to enhance quality control, data integrity and operational efficiency.

QLIMS is a lab grown modern, scalable and affordable Laboratory Information Management System (LIMS) that serves as a comprehensive platform for laboratory data management and workflow automation, particularly in genomics and sequencing environments. 

For more information, visit onqsoft.com

OnQ Software ǀ 6, 405 High Street, Northcote, Melbourne VIC Australia ǀ Phone  +61 3 8582 6999 ǀ info@onqsoft.com


Press Contacts

OnQ Software
Email: info@onqsoft.com
Phone: +61 3 8582 6999

 

How to Keep Genomics Labs Audit-Ready with QLIMS

Genomics labs

In genomics, accuracy is everything. From handling patient samples to reporting results, every step must be traceable and reliable. But for many labs, preparing for an audit is a stressful, resource-heavy process. Paper records, spreadsheets, and siloed systems often create gaps that auditors quickly uncover.

The solution is to make compliance part of daily operations rather than a separate task. That’s where QLIMS comes in, helping genomics labs stay audit-ready at all times, not just when the inspection notice arrives.

1. Built-in Electronic Signatures and Authentication

Regulations like HIPAA, and ISO standards require strict control over who accesses and signs off on data. QLIMS provides secure electronic signatures and user authentication, ensuring every action is verified. No need to track down handwritten notes or approvals, the system enforces compliance automatically.

2. End-to-End Audit Trails

Auditors need proof of what happened, when, and by whom. QLIMS automatically records every action from sample receipt and preparation to analysis, results, and reporting. These audit trails reduce the time and stress of audit preparation.

3. Quality Management Integration

Audits often focus on deviations, CAPAs, and approvals. With QLIMS, quality management isn’t an afterthought, it’s embedded in the workflow. Whether it’s tracking non-conformances or linking corrective actions to specific samples or tests, all data is stored in one system.

4. Secure and Compliant Cloud Hosting

Genomics labs generate enormous amounts of sensitive data. By running on AWS, QLIMS provides scalable storage, encryption, access control, and geographic compliance. This helps labs meet both local and international data privacy requirements without adding IT overhead.

5. Turning Insights into Action

Being audit-ready isn’t just about compliance, it’s about using the data to improve lab operations. With QLIMS, every record and test result is instantly available for analysis. Labs can monitor trends, identify potential bottlenecks, and make informed decisions faster. By transforming raw data into actionable insights, QLIMS helps genomics labs not only pass audits but also enhance efficiency, reduce errors, and ultimately deliver better outcomes for patients.

In fast moving fields like genomics and precision medicine, staying compliant isn’t just about avoiding penalties, it’s about building trust with patients, partners, and regulators. QLIMS empowers labs to maintain transparency, accuracy, and security, ensuring they are audit-ready every single day. Contact us today to learn more or book a demo.