Advanced Nutrition Ingredient Manufacturer Bioactive Science & IP Platform Māori-Led · New Zealand

Who we are.

Mānuka Performance is an advanced nutrition ingredient manufacturer — we take raw New Zealand honey and its by-product, bee dross, and turn them into validated, science-backed bioactive ingredients, consumer products, and licensable IP. We are not a honey brand. We are a bioactive science company that happens to use New Zealand honey as its primary substrate.

Our business runs across four connected pillars — consumer products, B2B ingredient supply, clinical R&D, and a bioactive data & IP platform — anchored by our own validation standard, MPS PolySure™, and manufactured toward pharmaceutical-grade (GMP) standard from Auckland.

58%
Blended gross margin
4
Compounding revenue pillars
3
Active export markets — USA, Korea, China
7
Certified polyphenols per batch (PolySure™)
Value Architecture

Two raw streams.
One validated system.

We take two overlooked, low-value raw inputs — honey and bee dross, its waste by-product — and move both up the value curve through validated processing stages, converging into a single family of high-value products and ingredients.

Honey Track
Raw Honey
Validated Bioactive Recipe
PolySure™ certified
Formulated Ingredient
gel & powder base
Dross Track
Raw Bee Dross
~20t/week discarded, NZ-wide
Solid-State Fermentation
proprietary SSF process
Validated Powder Ingredient
PolySure™ certified
Converges → Formulated, Validated Products
Both tracks feed the same finished-product and ingredient formats — sharing packaging, certification, and go-to-market channels.
Route 1
Bulk / B2B Ingredient Supply — incl. food service
Route 2
Branded Consumer (CPG) Products
Route 3
Licensed Formulation & Ingredient IP
Four Pillars, One Platform

Independent value.
Compounding together.

Each pillar can generate revenue on its own. Together, they reinforce each other — consumer revenue funds R&D, R&D produces defensible claims and data, and that data unlocks higher-margin B2B and licensing revenue.

Pillar 1
Consumer Products (CPG)
Revenue: branded consumer goods

GI-PRO™ and LiquidFuel™ — sold direct to consumers via Amazon, D2C, and retail. This is our most visible revenue line and our proof-of-market: it generates first-party sales data, brand equity, and real-world usage evidence that strengthens every other pillar.

Pillar 2
B2B Ingredient Supply
Revenue: bulk ingredients, incl. food service

Bulk and formulated ingredient supply to manufacturers, brands, and food-service operators — from 3kg dispense formats for cafés and events, through to contracted bulk supply for other nutraceutical and CPG companies. Higher margin, recurring, and contract-based.

Pillar 3
Clinical R&D
Feeds: claims, data, and commercial advantage

Ethics-approved trials, polyphenol validation science, and novel compound research don't generate direct revenue today — they generate the evidence that makes every other pillar more valuable. Every clinical result becomes a defensible label claim, a B2B credential, and a data asset.

Pillar 4
Bioactive Data Intelligence
Revenue: licensable IP

Our accumulated PolySure™ dataset, provenance mapping, and screening science becomes licensable IP in its own right — to industry, regulators, and research partners. This is the layer that turns a commodity ingredient business into a data and IP platform.

How the four pillars work together: Pillar 1 (consumer sales) generates cash flow and real-world usage data. Pillar 3 (R&D) turns that data, plus dedicated clinical trials, into validated claims and proprietary compounds. Those claims and compounds strengthen Pillar 2 (B2B contracts demand evidence before they'll sign) and become the raw material for Pillar 4 (licensable data and IP). Pillar 4, in turn, is what re-rates the whole business from a conventional consumer-goods multiple toward a data-and-IP platform multiple — and every dollar it generates is reinvested back into Pillar 3. It is one system, not four separate businesses.
Differentiation & IP Moat

Why this can't be
replicated offshore.

Our advantage isn't a brand story — it's structural. It sits in the science, the provenance, and the formulations, and it deepens every year through ongoing research.

Validation Standard
MPS PolySure™
An ISO 17025-accredited framework tracking seven key polyphenols per batch — caffeic acid, ferulic acid, quercetin, pinobanksin, chrysin, pinocembrin, and galangin. No other producer quantifies and certifies these seven simultaneously to accredited standard. It's the evidentiary basis for every label and ingredient claim we make.
Biological Origin
Provenance
Our polyphenol profiles are the direct expression of specific New Zealand ecosystems — soil, altitude, seasonal hydrology, and native flora that exist nowhere else. The supply chain cannot be relocated and the provenance cannot be manufactured. It's a biological fact, validated by science and held under Māori guardianship.
Formulation Know-How
Proprietary Processing
Our solid-state fermentation process for dross, and our formulation science for combining honey matrices with actives (probiotics, fruit extracts, BCAAs), represent years of accumulated process know-how that isn't published or patentable in isolation — but is very hard to reverse-engineer.

This moat compounds through ongoing work: an active RCT on gut microbiome outcomes, an MPI-funded polyphenol validation programme covering 100+ honey varieties, and an untargeted screening programme that has already identified ten putative novel compounds across 112 honey samples — candidates for future characterisation, reference standards, and patent-protectable IP. Every study adds another layer that a competitor without our data, our partnerships, and our provenance simply cannot replicate.

Markets — USA · Korea · China

Three markets.
One validated platform.

High-level Total Addressable Market (TAM), Serviceable Addressable Market (SAM), and Serviceable Obtainable Market (SOM) figures across our three priority export markets — conservative, bottom-up modelling built against current resourcing, not aspirational demand.

MarketCategory TAMSAM (addressable)SOM — Year 1SOM — Year 3
USA$40B–$80B~$3.2B–$4.8B$1.5M$12.6M
South Korea$0.7B–$6.9B~$95M–$550M$0.2M$0.7M
China$2.7B–$26.6B~$310M–$1.9B$0.5M$3.7M
Combined$2.2M$17.0M

USA spans the sports-energy/recovery category ($40B) and the broader nutraceuticals/functional-food category ($80B, including the emerging GLP-1 adjunct-nutrition segment). Korea spans sports/endurance ($0.7B) and the wider East Asian nutraceutical category ($6.9B). China spans CBEC-addressable wellness ($2.7B) and the broader nutraceutical category ($26.6B). SOM figures assume today's headcount, budgets, and manufacturing capacity — the binding constraint on growth is capital and production capacity, not market size or product readiness.

Manufacturing Scale

Auckland as the
production hub.

We are consolidating manufacturing and commercial infrastructure from the Bay of Plenty into Auckland — New Zealand's largest economic centre and most connected international gateway — building toward pharmaceutical-grade (GMP) production.

GMP
Pharmaceutical-grade manufacturing standard — the target certification
AKL
Auckland — production HQ relocation in progress
3 Markets
Simultaneous supply capability — USA, Korea, China
Licensable
PolySure™ is a revenue-generating licensable service — not open access

To be clear on positioning: MPS PolySure™ is not an open-access standard for the wider industry. It is our proprietary validation framework, and any future availability to other honey sector participants would be structured as a licensed, revenue-generating service — another expression of Pillar 4, not a shared public good.

Phase 1 · Underway
Relocation
Manufacturing consolidating from the Bay of Plenty to Auckland. Existing contract manufacturing and quality systems maintained through transition.
Phase 2 · Investment-Contingent
GMP Facility Design
Facility design and GMP regulatory pathway. Target: ISO-certified, HACCP-compliant facility serving consumer and B2B demand across three markets at once.
Phase 3 · Investment-Contingent
Full GMP Production
GMP production online. China CBEC and B2B ingredient supply at scale. Auckland as primary production hub for global export.
Phase 4 · Investment-Contingent
Innovation Centre
Facility evolves into a dedicated advanced nutrition R&D and innovation centre, with in-house analytical capability and licensable PolySure™ testing services.

Phase 1 is underway within current resourcing. Phases 2 through 4 — GMP facility build, full production scale-up, and the innovation centre — are contingent on the capital raise described below; timing and sequencing will flex to the pace of funding secured.

The Step Change

Not doubling the category.
Building the next one.

New Zealand's honey industry exports over $400 million a year — almost entirely graded on a single antimicrobial marker (MGO). We're building the science and commercial infrastructure to change that permanently, for the whole sector, not just for us.

Industry Today
Commodity Export
Single-marker MGO grading. Bulk export. Margin compression. Price-taker in global markets.
Mānuka Performance Today
Validated Platform
PolySure™-certified products. Clinical evidence. Active in USA, active exports to Korea, China entry underway.
At GMP Scale
Bioactive Intelligence
Licensable IP. Global B2B ingredients. GMP Auckland hub. A sector-wide validation standard other NZ honey producers can build on.
Where the Science Is Heading

From nutrition,
toward bio-medical.

Our R&D programme is deliberately structured to move up the evidence ladder over time — from consumer nutrition claims today, toward the kind of clinical and mechanistic evidence that opens biotech, biomedical, and longer-range drug-development pathways.

Today
Consumer Nutrition Claims
Ethics-approved RCTs on GI-PRO™ gut microbiome outcomes, mood/sleep, and endurance performance — plus an active RCT on LiquidFuel™ energy gel and athlete endurance performance — generating defensible label and ingredient claims.
Building Now
Compound Characterisation
Untargeted LC-HRMS screening has identified ten putative novel compounds across 112 honey samples — systematic characterisation is the pathway to reference standards and patent-protectable IP.
Emerging
Mechanistic & Cross-Species Evidence
Research extending into aged-care sarcopenia, gut-brain axis, and companion-animal and equine health — building the mechanistic evidence base a biomedical pathway requires.
Long-Range
Biotech / Biomedical Optionality
Characterised novel compounds, an international research alliance (Jinan University), and an accumulating clinical evidence base preserve long-range optionality toward therapeutic and drug-development pathways — without those pathways being required for the current commercial plan to succeed.

This is a deliberate sequencing choice, not a promise of a therapeutic outcome: consumer revenue funds the science, the science funds deeper characterisation, and deeper characterisation is what eventually makes a biomedical or pharma conversation possible — on a timeline measured in years, not quarters.

The Ask

USD $10M, via
Active Investor Plus / Invest NZ.

We are raising USD $10M in growth capital, structured as a direct investment through the Active Investor Plus (Invest NZ) Growth Category. This capital removes the single biggest constraint on everything shown above: every forecast in this document — the SOM figures, the manufacturing phases, the market activity — is a conservative, status-quo estimate, built against today's headcount, today's budgets, and today's production capacity. It is not a ceiling on what this platform can do. It is what we can do without this capital.

USD $10M
Growth capital target, via AIP Growth Category direct investment
GMP
Unlocks Phases 2–4 of Auckland production infrastructure
3 Markets
Accelerated B2B activation — USA, Korea, China
NZ IP
All IP, data, and guardianship retained in New Zealand
Where It Goes — 1
Production Infrastructure
Funds Phases 2 through 4 of the Auckland build-out — GMP facility design and certification, full production scale-up, and the innovation centre — none of which proceed on the current timeline without this capital.
Where It Goes — 2
Production Capacity & Scale
Removes the supply ceiling that today caps every consumer and B2B curve in our modelling — stock-build, equipment, and capability that let us fulfil demand rather than ration it.
Where It Goes — 3
USA, Korea & China Market Acceleration
Dedicated in-market activation across all three revenue lines simultaneously: B2B ingredient supply contracts, B2B food-service accounts, and CPG consumer growth (Amazon, D2C, retail) — converting pipeline conversations into signed contracts and sales on a materially shorter cycle than our current, single-resourced pace allows.
Where It Goes — 4
IP Capture & Data Platform
Deeper clinical trial coverage, novel compound characterisation, and PolySure™ licensing development — the pillar that re-rates the whole business, funded ahead of schedule rather than out of thin consumer-revenue margins.
The upside case: the $2.2M Year 1 / $17.0M Year 3 combined SOM shown earlier assumes no acceleration beyond what is already funded or in motion — the addressable markets themselves ($40B–$80B in the US alone) are large enough to absorb a materially faster ramp. With USD $10M removing the capacity and go-to-market constraints on all three markets simultaneously, our internal view is that Year 3 revenue could realistically move into the tens of millions rather than the low teens — the platform, the science, and the market access already exist; what has been missing is the capital to run at the pace the opportunity supports.
Off-Ramps & Exit Options

Multiple paths.
One compounding asset.

Because the platform generates value in more than one way — product, ingredient supply, and IP — it also supports more than one exit pathway.

Pathway A
CPG Acquisition
Premium nutraceutical and functional-food brands with validated science, ambassador networks, and international distribution attract acquisition interest from global CPG majors.
Pathway B
IP Licensing / Roll-Up
MPS PolySure™ and the broader bioactive IP platform are licensable globally to ingredient suppliers, food manufacturers, and wellness brands — value compounds as certifications and contracts multiply.
Pathway C
Public Listing
A validated science-and-ingredient platform with multi-country revenue, proprietary IP, and an authenticated provenance story is positioned for NZX, ASX, or NASDAQ listing at appropriate scale.