Time is Brain, a spin‑off from Germans Trias Hospital (Barcelona)providing advanced stroke care to +1.8M people, and pioneer in clinical trials shaping global stroke guidelines. Led by 3 neurologists, Alicia Martínez, Jaume Coll, and the Key Opinion Leader Antonio Dávalos, the company has developed BraiN20®: the first and only real-time, portable, AI-powered stroke monitoring medical device. Idetects salvageable brain tissue, increasing the number of patients candidates for treatment up to 15%, saving 60 to 140 minutes of time-to-treatmentleading to 26% increase in treatment success. 

23
remaining days
68 investors
Investment achieved
2.337.862€
Target
2.500.000€
Invested
93.5%
93.5% INVESTED
Maturity

Premarket/clinical phase

Premoney valuation

12.000.000

Estimated exit

2029

Sector

Medical devices

Equity offered

20%

Minimum investment

1.000

Barcelona flag
Equity L
Tax deduction
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Overview: Time Is Brain

Valuation 12.000.000
Estimated return x13
% Offered 20%
Estimated exit 2029

The only smart device capable of continuous, real-time brain monitoring, patented, validated, and backed by a strong founder team.

Clinical Proof: 93-100% positive predictive value for EVT outcomes, outperforming all existing triage methods. Validated technology: PROMISE trial (NCT04099615).

Defensible IP: Proprietary biomarker‑driven tech with global patents to 2040 and clinical validation via the PROMISE study (223 patients).

Protected by 4 patent families and 1 trade secret covering both hardware and software. Strong moat against new entrants.

10+ years of research: Founded on research begun in 2013 at Germans Trias Pujol Hospital (Barcelona). Incorporated 2020. TRL 7-8, nearing market readiness.

Strong global Key Opinion Leaders (KOL) network: backed by 40+ stroke KOLs worldwide. Clinical credibility accelerates hospital adoption and regulatory pathways.

Wide-open field: no direct competitor can match the combination of portability, real-time monitoring, and accuracy >a significant first-mover advantage.

Machine Learning (AI): Time is Brain trained their data models to increase the predictive value of the treatment outcomes, and to be able to distinguish between different types of stroke.

Team and company culture: strong founder team and a company culture that is focused on impact, continuous improvement, diversity, and putting in the effort.

Ready to launch in EU and US: CE certification is expected in Q2 2026. The 510k FDA approval is expected in Q4 2026 to launch in the US in 2028.

Why now? In stroke, every second counts, answers can’t come too late

Despite the progress of Endovascular Thrombectomy (EVT), a highly effective, time-sensitive, minimally invasive procedure to remove large blood clots from brain arteries during an Acute Ischemic Stroke (AIS), stroke care still loses its most valuable asset: time. From the first emergency call or ambulance arrival, patients are moved toward a hospital, but ambulances function like transport buses: no neurological capability, no real‑time brain data. Critical minutes pass while the brain remains unmonitored, imaging isn’t yet available, and teams can’t confirm treatment eligibility, driving irreversible damage and poorer outcomes.

BraiN20® changes the equation. It is the only real‑time, continuous brain‑viability monitor that travels with the patient across the entire pathway (from ambulance to ER, angio‑suite and ICU) turning the diagnostic delay window into actionable, objective information.

Redefining the “Patient Journey”: From reactive diagnosis to precision intervention

BraiN20® is not just a device; it is the new standard transforming every critical stage of the stroke patient pathway:

  • Objective triage in the Ambulance & ER: Currently, triage relies on subjective clinical scales. BraiN20® enables an objective diagnosis in just 33 seconds, immediately identifying candidates for endovascular treatment (EVT). This accelerates direct transfer to the appropriate center, avoiding vital time loss and allowing for continuous monitoring during transit. Furthermore, BraiN20® is so intuitive that any technician can operate it without the need for complex training.
  • Live functional guidance during EVT: For the first time, interventional neurologists have a “real-time functional map” during thrombus extraction. BraiN20® immediately detects whether reperfusion is effective or if complications arise, increasing the procedure’s success rate by 26%.
  • Continuous bedside surveillance post‑procedure: Monitoring does not end in the operating room. BraiN20® provides bedside surveillance to detect re-occlusions or early deterioration long before symptoms become visible, enabling an immediate medical response and protecting the salvaged brain tissue.

Bottom line: We move from passive waiting to real-time visibility. From minute one, we see exactly what the brain needs. This is the inflection point to transform outcomes, slash system costs, and set the new global standard of care.

BraiN20®: The “ECG for Stroke” for continuous brain monitoring

Our patented technology provides instant access to brain health through:

  • N20 Signal Recording: A clinically validated biomarker based on a brain signal that reflects the functional status of broad cortical regions. The N20 originates from the brain’s Somatosensory Evoked Potentials (SEP) — electrical responses generated when the median nerve is stimulated. As the earliest cortical arrival of that signal, its presence and quality serve as a robust marker of cortical viability in acute neurological conditions, as demonstrated in the PROMISE clinical study (for more information please refer to “The project” section).
  • Outcome‑Prediction AI: Proprietary software that predicts patient prognosis with 93% sensitivity before treatment and 100% during EVT, outperforming conventional imaging when time matters most.
  • Portable, non‑invasive hardware: Single‑use stimulation and recording components designed for any setting: ambulance, ER, angio‑suite, or ICU.

Key advantages & market potential

  • Clinical efficiency: Cuts time‑to‑treatment by up to 140 minutes and optimises patient flow, routing candidates directly to EVT‑capable centers from the ambulance.
  • Economic impact: Targets a massive human and economic burden; stroke‑related disability drives €891B in global annual costs.
  • Tier‑1 validation: Supported by the PROMISE clinical study (223 patients), backed by 40+ KOLs and 13 hospitals.
  • Strong IP: A robust patent portfolio protected through 2040.

World‑class team & executable plan

Time is Brain is a spin‑off of Germans Trias Hospital, pioneer and architect of Spain’s national Stroke Code. The company is led by stroke‑specialist neurologists Alicia Martínez, MD, PhD Jaume Coll, MD, PhD and global KOL Antonio Dávalos, MD, PhD, combining frontline clinical leadership with seasoned MedTech business execution.

With CE mark and U.S. market entry (FDA) expected during 2026, Time is Brain is positioned to transform global neurovascular care and generate significant returns through a strategic M&A pathway.

Since inception, the company has raised €1.8M in equity and €4.2M in non‑dilutive public funding, including the EIC Accelerator. Time is Brain is currently opening a €2.5M round, with ~2M€ already committed, to:

  1. Complete the FDA dossier,
  2. Execute the EU commercial launch, and
  3. Prepare U.S. market entry
In Capital Cell's own words

Time is Brain is addresses the most critical bottleneck in acute stroke care: the lack of real-time data on brain viability. Current medical protocols rely on static CT or MRI “snapshots” which, create delays and leaves patients unmonitored during their journey. Their device functions as an “ECG for the brain,” providing continuous, AI-powered insights into the brain’s electrical activity from the first point of medical contact, enabling a “direct-to-surgery” model that bypasses traditional triage.

The science behind the platform is centred on their proprietary N20 biomarker, able to predict patient outcomes after thrombectomy. This approach was validated through the PROMISE clinical trial (in over 160 patients), which proved superior predictive accuracy compared to standard imaging. Crucially, the platform is scalable into ICUs to eliminate neurological “blind spots.” With an international patent portfolio, CE Mark and FDA clearance targeted for 2026, major regulatory risks are mitigated.

Market access is exceptionally de-risked. Co-founder Dr. Antonio Davalos authors international stroke guidelines, giving the team the unique authority to integrate BraiN20® into standard clinical protocols for non-discretionary, recurring hospital adoption. Now backed by ‘The Foundry’ VC, adding vital supply chain and logistics expertise, the company is structured for commercial scale and a high-value exit.

Minimum investment: 1.000
Type of exit expected: M&A
Drag-along rights
Tag-along rights
Preferential liquidation rights
Anti-dilution rights
Tax deductions
Main risks

The company’s primary challenge lies in expanding its clinical evidence that BraiN20™ improves real-world stroke outcomes and decision-making. From a regulatory standpoint, their US strategy might delay full stroke-specific commercial claims. Commercially, early adoption may rely on hospital budgets rather than clear reimbursement, especially in the US. Finally, they face steep competition entering an ecosystem dominated by mature imaging platforms and large neurovascular incumbents.