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From validated technology to repeatable production

MyantX advances a validated material or process to repeatable production — pilot batches, then full runs, all on one campus.

Campus
170,000 sq ft
Pilot plant
20–1,200 L
Production
≤ 20,000 L
Reactors, process lines and overhead crane on the MyantX advanced-manufacturing floor

What scale-up covers

Engineering, piloting, and proving a process until it can run at volume — batch after batch.

Feasibility & techno-economics

Feasibility & techno-economics

A manufacturing-feasibility and techno-economic view — whether the process can scale, and whether yield, throughput, and cost work — before any capital is committed.

Process engineering

Process engineering

Turn a laboratory procedure into a controllable, repeatable process — handling, mixing, reaction, forming, and downstream steps.

Pilot production

Pilot production

Run representative batches at pilot scale to prove the process behaves before committing to volume.

Comparability & consistency

Comparability & consistency

Measure the scaled material against the bench benchmark, held to defined parameters and acceptance criteria — so what ships matches what was validated.

Technical transfer

Technical transfer

Package the process — operating sequence, batch records, and risk controls — to move it to another team or site.

Manufacturing & supply

Manufacturing & supply

For eligible processes: production campaigns, toll manufacturing, or ongoing supply — confirmed per program.

How we scale a process

Six stages, run as one program — starting from whatever already works, and built around repeatability.

  1. 01Assess

    Review the process, materials, equipment, hazards, and target volumes — and whether scale-up is technically and economically feasible.

  2. 02Define the strategy

    Establish the production pathway, the experimental and analytical plan, quality criteria, and milestones.

  3. 03Engineer the process

    Develop the operating sequence, material handling, equipment settings, parameters, and documentation for controlled execution.

  4. 04Pilot & characterize

    Run representative pilot batches, measure process and material behavior, and compare against the bench benchmark.

  5. 05Demonstrate repeatability

    Refine the process, establish operating ranges, confirm the agreed criteria, and document the risks and controls.

  6. 06Establish the production route

    Prepare the agreed transfer, manufacturing, supply, or extended-pilot pathway — not every program reaches production.

From the bench to full production

One campus carries a material from a few grams at the bench to full production runs — the same team and the same building at every scale.

An operator at an industrial knitting machine control panel on the production floor

Grams

Material R&D — AI modeling, analytical & design labs

Kilos

Scale-up & process optimization

20–1,200 L

Pilot production — modular pilot plant

1,200–20,000 L

Large-scale production — Supplies Development Center

Sectors we manufacture for

Process development and manufacturing for advanced materials, across the industries that put them to work.

AerospaceAutomotiveHealthcareConsumer electronicsClean techEnergy storageAdvanced filtrationAdvanced coatingsCosmeticsAgriculture

Quality & compliance

Manufacturing runs within Myant's certified management systems, with product-specific regulatory records maintained per program.

  • ISO 9001:2015Quality management
  • ISO 14001:2015Environmental management
  • ISO 45001:2018Occupational health & safety
  • Health Canada Establishment Licence #106352Medical devices, Class II
Quality & regulatory records 

Why scale up with MyantX

Staying repeatable as volume grows is the hard part. MyantX runs material R&D, testing, and the line as one operation — so what ships is what was validated.

  • The same team, end to end

    The team that scales your process works alongside the material R&D and the analytical lab — nothing is handed to a factory that has to relearn it.

  • Know before you commit

    A manufacturing-feasibility and techno-economic assessment shows whether a process can scale — and whether the economics work — so capital goes in only once the numbers hold up.

  • Honest about the limits

    Equipment fit, usable volume, safety, and available capacity are confirmed up front. Not every process is eligible, and we say so.

Frequently asked questions

Not seeing your question? Talk to the team that would run your program.

Discuss a project 

Can you tell us whether scaling up is even worth it?

Yes — a program can start with a feasibility and techno-economic assessment, so capital goes into scale-up only once the technical and commercial case holds up.

Can you scale a process developed elsewhere?

Often, yes. We review the formulation or process, its documentation and sample data, hazards, and IP constraints to determine whether a transfer or scale-up program is feasible.

What pilot and production volumes are available?

Modular pilot lines run from 20 to 1,200 L and production up to 20,000 L. The right range for your process is confirmed during scoping, against technical fit and availability.

Do you offer toll manufacturing or ongoing supply?

For suitable processes, yes. The manufacturing model, campaign size, specifications, quality requirements, and commercial terms are all defined during scoping.

Can the process be transferred to another site?

Where included in the engagement, we can prepare an agreed technical-transfer package and support transfer into a client or third-party manufacturing environment.

How are hazards, quality, IP, and timing handled?

Hazards and handling controls are reviewed before work is accepted; quality requirements are agreed up front; and confidentiality, background and new IP, and transfer rights are set in the agreement. Timing depends on the starting process and the pilot iterations it needs.

Take it to volume

Tell us what currently works and what scale you need to reach. The team will help define the pilot, transfer, or manufacturing pathway.