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Investor information

Building pharmaceutical infrastructure from one focused product

NEUVIOR is building an integrated pharmaceutical company from a focused first product. PHARMORIS addresses the gap between evidence, decision, ownership and governed execution.

INVESTOR CONTEXT / PUBLIC RECORD

External context and project support record. This is not company performance.

Founder thesis

The investment case begins with proving institutional demand for a focused workflow before widening the company.

NHSBSA England cost context increases from £16.15bn in 2020 to £22.16bn in 2025. NEUVIOR has been selected for non-dilutive support for defined project work. Published award records are source linked. Award ceilings, eligible project costs, company contributions and cash received are different figures; none is customer revenue, equity raised, adoption or an outcome. These figures are external context and a source linked company record, not company performance.
Review the full accessible data
Current product | PHARMORISCommercial test | Repeatable institutional demandBoundary | External context is not company performance

Investment thesis

Begin with the operating gap institutions must solve.

PHARMORIS is intended to help authorised medicines teams move from evidence and prioritisation to accountable ActionCases, governed decisions, activity, blocker management and review.

The immediate commercial test is whether institutional buyers confirm the problem, pay to evaluate the workflow and accept the value model.

01

Problem

Evidence does not reliably become owned and reviewable action.

02

Focused product

One configurable, human governed medicines operations product.

03

Expansion

Adjacent pharmaceutical capability only after the first product is repeatable.

Commercial discipline

Progress depends on paid evidence, not presentation.

NEUVIOR intends to avoid unpaid pilots and customer specific product forks. An evaluation should be paid, time limited, governed and linked to a defined contracting decision.

Human decision requiredProceed only inside an evidenced and governed scope.
01

Buyer confirmation

The responsible institution recognises the problem and intended value.

Continue condition
02

Paid evaluation

The scope, evidence, decision date and success measures are explicit.

Continue condition
03

Repeatable delivery

Configuration and assurance can be reused without a customer specific fork.

Scale condition

Product evidence

See what is built. See what still needs proving.

PHARMORIS is NEUVIOR's current commercial focus. The controlled Demo40 workflow shows how public source evidence can become a source linked ActionCase, a named human review and an auditable record.

The purpose is not to automate authority. It is to make the next decision easier to inspect, challenge and govern.

Controlled Demo40 snapshot

A dated product evidence ledger.

Reviewed 4 August 2026

The demonstration source timestamp is 16 July 2026. These counts are not production performance measures.

01
3
Source linked ActionCases
02
3
Evidence rows linked
03
8
Linked evidence items
04
3
Human reviews required
05
0
Patient data feeds
06
0
Realised value evidence

Source qualification

A source becomes useful only after it becomes governable.

Discovery is the start of diligence. It is not evidence of an integration. Every future source should pass a visible sequence before it can support live work.

  1. 01

    Candidate source research

    Identify a potentially relevant source without treating discovery as permission or connectivity.

  2. 02

    Rights and access check

    Confirm the rights, licence, lawful basis and technical route needed for the intended use.

  3. 03

    Source receipt

    Record what arrived, when it arrived, its scope and any material limitation.

  4. 04

    ActionCase

    Create governed work only when the source, assumptions and decision need remain visible.

  5. 05

    Named human review

    Name the accountable reviewer. Keep the decision with an authorised person.

  6. 06

    Audit record

    Preserve the source, review state and decision history for later inspection.

Next proof

The questions that should determine what comes next.

  1. 01

    Will a responsible buyer fund a time limited operational test?

  2. 02

    Can the workflow be configured without a customer specific product fork?

  3. 03

    Can the buyer validate value, safety and implementation evidence locally?

  4. 04

    Does the test progress to repeat procurement?

Risk boundary

What the public record supports. What remains to prove.

AreaWhat the public record supportsWhat remains to prove
ProductA controlled source linked demonstration with human review.Production readiness and independent assurance.
CommercialA defined route from product review to a paid evaluation decision.A signed buyer contract and repeat procurement.
ValueProjected opportunities remain visibly labelled as projected.Independently reviewed evidence of realised value.
DataPublic source evidence and zero patient data feeds in the controlled demonstration.Approved and lawful data access for any future live scope.
ExpansionPHARMORIS is NEUVIOR's current product focus.Evidence that supports investment in each later capability.

PUBLIC DATA / SOURCE CHECKED 20 JULY 2026

Investor context and public record

External context and project support record. This is not company performance.

FIGURE A / NHSBSA

Estimated cost to NHS commissioners before central rebates

England, calendar years 2020 to 2025

Line chart showing the NHSBSA England total increasing from £16.15bn in 2020 to £22.16bn in 2025.

NHSBSA Table 1 total using actual costs for items dispensed in the community and actual hospital and Adult Secure Estate costs. NHSBSA uses the term medicines as a publication shorthand that also covers appliances, dressings and medical devices. This is health system expenditure context. It is not avoidable spend, NEUVIOR TAM, revenue, savings or traction. Published 2 July 2026; source checked 20 July 2026.
England annual cost context data
YearExact GBPDisplay
202016,150,103,693.7714£16.15bn
202117,504,726,814.6583£17.50bn
202218,481,660,799.5121£18.48bn
202320,221,015,312.1001£20.22bn
202421,255,229,398.1745£21.26bn
202522,162,066,435.2205£22.16bn

FIGURE B / NHSBSA

Estimated cost by prescribing and dispensing setting

England, calendar year 2025

Comparison showing £11.43bn for Hospital prescribing issued within hospitals and £10.56bn for Primary care prescribing dispensed in the community, with three smaller settings listed separately.

NHSBSA actual cost setting breakdown. Setting expenditure does not establish inefficiency, avoidable cost, savings or a PHARMORIS opportunity. The Adult Secure Estate calendar year summary uses the previous financial year figure, as documented by NHSBSA. Published 2 July 2026; source checked 20 July 2026.
2025 cost by setting data
SettingExact GBPDisplay
Hospital prescribing issued within hospitals11,429,956,273.5705£11.43bn
Primary care prescribing dispensed in the community10,558,085,676.11£10.56bn
Hospital prescribing dispensed in the community111,117,697.31£111.1m
Dental prescribing dispensed in the community35,143,788.23£35.1m
Adult Secure Estate27,763,000£27.8m

FIGURE C / OLS

UK life sciences subsector context

Office for Life Sciences estimates, 2023/24

Three paired comparisons showing biopharmaceutical and medical technology turnover, employment and company counts in the Office for Life Sciences 2023/24 estimates.

Office for Life Sciences estimates from official statistics in development. The 2023/24 methodology differs from 2021/22 and earlier estimates; company geography may reflect a registered administrative address rather than physical activity. The figures are sector context and not NEUVIOR TAM, market share, revenue, competition or forecast. Published 2 October 2025; source checked 20 July 2026.
UK life sciences subsector context data
MeasureBiopharmaceuticalMedical technology
Turnover£98.9bn£48.0bn
Employment163,600196,000
Companies2,9604,360

FIGURE D / PROJECT SUPPORT

Support without equity dilution

Source linked project support ledger. No aggregate funding total is presented. Published award values, eligible project costs, company contributions and cash received remain distinct.

Source linked project support with no aggregate funding claim

NEUVIOR has been selected for non-dilutive support for defined project work. Published award records are source linked. Award ceilings, eligible project costs, company contributions and cash received are different figures; none is customer revenue, equity raised, adoption or an outcome.
Project support breakdown data
Funding componentProvider and basisPublished valueStatusSource
VIONIX ZEROInnovate UK · Published grant award£25,000AwardedUKRI project 10180575
PHARMORISInnovate UK · Published grant award£49,928AwardedUKRI project 10173524
SMART:SCOTLANDScottish Enterprise · Published reportingPublicly reported supportPublicly reportedTheBusinessDesk.com public award record

External context is not NEUVIOR market size, traction, revenue, customers, deployment, adoption, savings or outcomes.

Classified public record

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QUESTIONS · ANSWERED DIRECTLY

The useful answers, in one place.

Browse every question
01What non-dilutive support has NEUVIOR been selected for?

NEUVIOR has been selected for non-dilutive support for defined project work. The public record links to the published project level sources without presenting an aggregate total.

02Does a published award value mean all cash has been received?

No. Published award records are source linked. Award ceilings, eligible project costs, company contributions and cash received are different figures; none is customer revenue, equity raised, adoption or an outcome.

03Why does NEUVIOR not publish one aggregate support figure?

A single total can mix award ceilings, eligible project costs, company contributions and cash received. NEUVIOR therefore links the already public project records and keeps those definitions separate.

04Does grant support prove adoption or approval?

No. A grant award supports defined innovation work. It does not itself prove a product is deployed, approved, commercially adopted or delivering an outcome.