JANUARY 2027 LAUNCHING OPERATIONS (UK | USA | UAE)

Innovative medical interventions face a systemic bottleneck to reach the patients who need them. Verada works on bridging them !

Verada is the research and operations layer for innovative interventions entering the UK | USA | UAE regions. We support innovative medical interventions (devices and medicinal products) across neuro, musculoskeletal, and cognitive care, from clinical research protocols, regulatory strategy through to real-world evidence for clinical, operational and commercial adoption.

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The Adoption Gap

Approval is not adoption

In medical innovation, earning a UKCA or CE mark should be the beginning of a technology's clinical life. Too often it's where progress stalls, proven interventions stranded on the wrong side of a fragmented, risk-averse system while patients lose the treatment windows that matter most.

The adoption valley R&D & trials Proven abroad CE / UKCA mark Approval earned… No evidence → no adoption Verada bridge Adoption at scale NHS & private clinics
Where it stalls
Following CE or UKCA marking, adoption depends on procurement processes that are fragmented across providers and on commissioning decisions that require local real-world evidence. That evidence can be generated only through deployment, which has not yet occurred.
How Verada addresses it
The intended model is to support regulatory entry, deploy the technology within Verada's own care delivery, and generate the clinical, operational and health-economic evidence that commissioning decisions require.
Adoption at scale
That evidence is a precondition for provider purchasing and for public healthcare commissioning. It is not sufficient on its own.
The Group

Three functions, one discipline

Healthcare runs on numbers nobody actually measured. What a new technology costs to deliver is estimated. How a patient's motor or cognitive state changed is rated by a clinician, on an ordinal scale, a handful of times a year. Rehab Clinics measures what it genuinely takes to run a proven technology in the UK, and publishes it. Clinical Research gives trial sponsors objective, continuously captured endpoints where none currently exist. Healthcare IT makes both defensible enough for a regulator, a payor or a sponsor to rely on.Three buyers. One discipline: measure what the rest of the field estimates.

Verada Group

Strategy & oversight

The connective layer that holds everything together: group strategy, market-access direction, evidence governance, and the shared clinical infrastructure every company reuses. It's what lets each new technology follow the same proven route rather than starting from zero. Beneath it sit three focused operating companies:

Operating companies
Coming soon

Verada Healthcare IT

The platform & data engine

The unifying layer that brings together multimodal data across care settings and clinical trial units. It identifies and characterises real-world patient cohorts from routine EHR data, captures the full spectrum of trial outcomes (patient-, clinician-, and performance-reported), and structures it all into evidence-ready clinical intelligence: the backbone the whole group runs on.

InteroperabilitySemantic & syntactic
CoverageDevice- & vendor-agnostic
Platform · Data · Clinical AI
Explore Healthcare IT →
Coming soon

Verada Clinical Research

Decentralised clinical trials

A next-generation Clinical Trials Partner running decentralised trials across neuro/CNS, musculoskeletal, and cognitive indications. It spans devices, small molecules, biologics, and ATMPs (cell & gene therapies), plus nutraceuticals and nootropics where they target cognitive endpoints, capturing molecular, physiological, psychological, and functional outcomes.

Medical DevicesTRL 5+
Medicinal CompoundsPhase II+
Neuro/CNS · MSK · Cognitive
Explore Clinical Research →
Coming soon

Verada Rehab Clinics

The first UK deployment

A CQC-registered service (expected by Jan 2027) treating neuro/CNS, musculoskeletal and cognitive conditions. We adopt internationally proven technology without waiting for someone else to move first, then publish what it actually takes to run it. Clinical outcomes show that a device works. Utilisation, staffing, throughput and payback are what make the next clinic buy one.

StagePost-approval, Pre-scale
EvidenceOperational · Economic
Neuro/CNS · MSK · Cognitive
Explore Rehab Clinics →
The Compounding Advantage

How the three functions interact

The group's defensibility isn't in any single layer: it's in the interlock. Delivering care generates exclusive, longitudinal rehabilitation data. That data sharpens the models and clinical protocols. Better outcomes win the trust of payers and open channel access. And that access drives more delivery.

Every turn of the loop deepens all of it at once: data that can't be acquired retrospectively, evidence in the formats commissioners already trust, and a route to market that gets harder to replicate with each patient treated.

The moat widens with volume rather than eroding under competition, because the advantage is built from the care itself.
A Repeatable Pathway

A repeatable sequence across the portfolio

The hard work is done once and amortised across the whole portfolio. Each new medical technology follows the same repeatable route, reusing the clinical infrastructure, evidence engine, and market-access playbook already in place.

1

Prepare

Study design, evidence-pathway build, and grant navigation: completed before first patient contact.

2

Validate

Feasibility and acceptability studies that qualify the intervention, de-risk workflow fit, and prepare higher-order trials where warranted.

3

Deploy

Clinic-led patient deployment within Verada's own care delivery: generating revenue, operational data and clinical outcomes concurrently.

4

Scale

Real-world clinical and operational evidence unlocks the route to market: Real-world evidence supports private-provider purchasing, payer engagement and public healthcare commissioning where evidence supports it.

The People

Clinical, Regulatory, and Technical depth

Verada is led by a team spanning healthcare delivery, medical-device regulation, rehabilitation science, and health-data governance, bringing together the clinical, regulatory, and technical depth the group runs on.

Management Team
DP
Dilip Chakravarthy Pasupuleti
Founder & Chief Executive Officer
VC
Vidhyasree Chandu
Co-Founder & Chief Regulatory Affairs Officer
SK
Dr. SureshKumar Kamalakannan
Clinical Director, Rehabilitation & Occupational Therapy
SS
Sailaja Swamisetti
Consultant, Data Protection Lead (IP, GDPR & Health Data)
Progress

Progress so far

Verada is de-risking ahead of build, securing partners and non-dilutive funding before any private capital is raised. Early progress across the group:

Signed

Anchor partnerships

2 device-partner MOUs signed

Memoranda of understanding with two proven medical-device partners, establishing Verada's first technologies for UK adoption.

Confirmed

Academic collaborators

2 university research partners

Working with Northumbria University and the University of the West of England, Bristol on our feasibility programme.

In progress

Public, non-dilutive funding

£3.3M applied for — outcomes pending by Oct 2026

Public funding sought to support our initial feasibility study, validating the model with non-dilutive research funding ahead of any private raise.

The Offer

What partners get

Approval proves a technology works. It does not tell a clinic director how many sessions a week they can run, what grade of therapist they need, or when the investment pays back. Those are the questions that stall adoption, and they can only be answered by someone willing to run the service first.

For device manufacturers

You have the mark. You don't have UK scale.

We become your first UK site, at our own commercial risk, and turn going first into a package that lets the next twenty clinics go second.

  • A named reference site treating real patients under a registered provider
  • Operational proof — utilisation, throughput, therapist grade, training time, completion and dropout
  • Economic proof — cost per session, revenue per session, payback period, budget impact
  • A deployment blueprint — protocols, patient selection criteria, SOPs, therapist training curriculum
  • Clinicians who take a peer's phone call and say what it was actually like
Not yet UK-approved? We partner on grant-funded feasibility, RCT and health-economic work packages, so your route to a UKCA mark is funded non-dilutively.
For trial sponsors

Your comparator arm is unmeasured. Ours isn't.

Rehabilitation is the largest uncontrolled variable in neuro and MSK recovery trials, and ordinary sites cannot fix it. We deliver it to protocol and evidence that we did.

  • Protocolised delivery, identical across every participant and every session
  • Objective capture — EMG, EEG and range of motion recorded, not self-reported
  • Dose and adherence quantified per repetition, per session, per participant
  • SynPhNe and Pheezee as ePerfO instruments across neuro, MSK and orthopaedic interventions
Decentralised trial delivery through Verada Clinical Research, from exploratory endpoints upward.
Check applicability

Three questions. Returns the relevant instrument and the principal limitation.

For Investors & Partners

Investment and partnership

Verada is building infrastructure at the intersection of medical technology, regulated care delivery and clinical evidence generation. The model is intended to accumulate value with clinical volume, though it is pre-revenue and that has not yet been demonstrated. Enquiries from health technology investors, prospective partners and collaborators are welcome.

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Get In Touch

Enquiries

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