QLIFENasdaq StockholmMedical DevicesIFRS · SEK

QLife Holding

Qlife Holding AB is a Swedish diagnostics company built around the Egoo platform for decentralized biomarker testing. Through its subsidiary Egoo Health ApS, the group develops and commercializes home-use and point-of-care tests, devices, and consumables for blood-based health monitoring.

Revenue0.3m SEK
+264.0 %y/y
Operating profit (EBIT)-19.4m SEK
+65.0 %y/y
EBIT margin-5,982.7%
+56,210.5 ppy/y
Net income-20.6m SEK
+63.3 %y/y

Fiscal year 2025 · change from previous year

Development 2022–2025

-200-150-100-50050m SEK2022: 18 m SEK2022: EBIT -87 m SEK20222023: 0.24 m SEK2023: EBIT -157 m SEK20232024: 0.09 m SEK2024: EBIT -55 m SEK20242025: 0.32 m SEK2025: EBIT -19 m SEK2025TTM 2026: 0.86 m SEKTTM 2026: EBIT -20 m SEKTTM0.86-20
RevenueOperating profit (EBIT)TTM = last 12 months, not a full fiscal year

Business

Share of revenue
Diagnostic devices35 %

Analyzer hardware used to run decentralized blood tests.

Test capsules and consumables45 %

Single-use cartridges and consumables used with the Egoo system.

Clinical and regulatory development10 %

Validation work and product development supporting market approval.

Service and support10 %

Ancillary services tied to product deployment and customer use.

Customers

Qlife sells to users and partners in decentralized diagnostics, including consumers managing chronic conditions, healthcare providers, and commercial partners evaluating the platform. The company also engages with IVD, pharmaceutical, and consumer health companies that may use the technology for collaboration, distribution, or commercialization.

Home users with chronic conditions

Buy Egoo tests for convenient biomarker monitoring outside traditional labs.

Pharmacies and retail health channels

Offer in-store blood testing and related consumables to drive repeat usage.

Healthcare providers and hospital-at-home programs

Use decentralized testing to support remote monitoring and care pathways.

Strategic industry partners

IVD, pharma, and consumer health companies evaluate the platform for partnerships.

Strategy

Qlife is focused on commercializing decentralized diagnostics through the Egoo platform, with emphasis on regulatory milestones, product validation, and partner-led market access. The company is also pursuing pharmacy-based testing and strategic partnerships to broaden distribution and support recurring use of its consumables.

Regulatory approval and validationShort term

Clinical and regulatory clearance is required before broad commercialization.

Strategic partnershipsShort term

Partners can accelerate distribution, credibility, and market reach.

Pharmacy and retail channel expansionMedium term

Retail testing can increase access and testing frequency.

Recurring consumables modelMedium term

Test capsules can create repeat revenue tied to platform usage.

Geography

Qlife is headquartered in Göteborg, Sweden, and reports through a Swedish parent company with Danish subsidiary Egoo Health ApS. Its commercial focus has included Scandinavia and the UK, with additional activity and partner discussions referenced in China and other international markets.

Risks

Qlife’s business depends on successful clinical validation, regulatory approvals, and partner execution before products can scale commercially. As a development-stage diagnostics company, it also faces financing, dilution, manufacturing, and market-adoption risks typical of regulated medtech businesses.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Regulatory approval delays1Financing and dilution risk2Partner and commercialization risk3
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Regulatory approval delaysImpact: HighLikelihood: High

    Products cannot be broadly marketed until validations and approvals are obtained.

    Exposure: Egoo tests and new biomarker launches

  2. Financing and dilution riskImpact: HighLikelihood: Medium

    The business is capital intensive and may need additional funding to continue development.

    ExposureEquity issuesWarrantsLoan-linked instruments
  3. Partner and commercialization riskImpact: MediumLikelihood: Medium

    Market access depends on third-party partners and channel execution.

    Exposure: Hipro partnership and pharmacy rollout

  4. Manufacturing and purchasing riskImpact: Medium

    Diagnostic products require reliable production of devices and consumables.

    ExposureAnalyzerCapsulesTest supply chain
  5. Intellectual property and competitionImpact: Medium

    Competing diagnostics platforms and IP disputes can limit adoption and pricing power.

    Exposure: Home diagnostics and biomarker testing

Accounting

Judgemental items
IFRS 15 revenue recognition

Revenue is tied to transfer of control for devices and consumables, so shipment timing matters.

Impact: Quarterly revenue can fluctuate materially on small volumes

Capitalized development costs

Internally generated intangible assets depend on technical feasibility and future benefit assumptions.

Impact: Affects operating expenses, assets, and future amortization

Impairment of intangible assets

Development assets not yet in use are tested for impairment annually or when indicators arise.

Impact: Can create non-cash write-downs if commercialization assumptions weaken

Lease accounting under IFRS 16

Right-of-use assets and lease liabilities affect reported leverage and depreciation.

Impact: Changes balance-sheet presentation and operating cost profile

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026

QLife Holding (QLIFE) Revenue, Earnings & Financials 2025 – Clarifo