Cut battery costs. Catch failures early. Ship higher-performing product to your customers.

What it is

Acceptance criteria come from two places: what your cell manufacturer warranties, and what your application actually demands. A drone battery isn't a power tool battery isn't a medical device battery. The criteria are the bar a cell has to clear to make it into your product.

How Micantis helps

• Consult on test design. We help translate the warranty and your application into criteria that match how the cell will actually be used.
• Document every spec in one place. Criteria, revisions, and approvals all live in the platform, not in scattered spreadsheets.
• Auto evaluate every test once the criteria are written down. Pass, fail, or borderline, decided the moment data lands.

What it is

A test protocol is the recipe — what you'll actually do to verify the cells. Cycle life, cold testing, capacity checks, abuse tests. It also decides how many cells you'll test out of the batch, since most teams can't afford to test every cell in every shipment.

How Micantis helps

• Help design and write your cell protocols. Cycle life, cold cycling, capacity, abuse, sampling strategy, all tuned to your application.
• Save test procedures in Micantis and automatically apply them to every new shipment, so you're not rebuilding the test plan every time cells arrive.

What it is

Most product companies can't test every cell in every shipment, the volume is too high and the cycle time is too long. You need a representative sample, big enough that the result is statistically meaningful and small enough that the rest of the cells can ship into product. Done right, the sample tells you whether the batch as a whole meets the criteria you defined.

How Micantis helps

• Help size and select samples that match your criteria, your batch volumes, and your risk tolerance.
• Auto generate test requests the moment a shipment arrives, so the sampling plan runs the same way every time.
• Track sample to batch decisions so the sampling strategy is documented and defensible in an audit.

What it is

Once the protocol is set, somebody has to actually run the tests. Either in your own lab, or at a partner lab if you don't have the equipment. Most product companies don't have a battery lab — and don't need one if they have the right partners.

How Micantis helps

• Connect you with battery testing partners if you don't have your own lab, or to handle overflow and specialty programs.
• Automatically import test results from in-house or external testing, across 50+ cycler formats.
• Automatically check if each cell passes or fails the criteria you set, the moment the data lands.

What it is

Every shipment of cells has to be decided on. Ship into product, hold for review, or send back to the supplier. Without a system, this becomes a gut feel call. With one, it's grounded in real test data and supplier history.

How Micantis helps

• Pass / fail evaluation against your spec, automatic
• Supplier history on every batch decision
• ML predictions for cells you can't test to completion

What it is

Suppliers will tell you they shipped you A grade cells. Your independent test data either confirms that or it doesn't. Either way, you now have a fact based conversation with them instead of an argument.

How Micantis helps

• Supplier scorecards with batch level metrics
• Trend tracking over months and quarters
• Shareable reports for supplier reviews

What it is

Depending on your industry, you'll face FDA, ISO 13485, DO 311A, NDAA, UL 9540, EU Battery Passport, or another audit. They all want the same thing: evidence. Every cell, every test, every decision, with a paper trail that holds up under scrutiny.

How Micantis helps

• Immutable audit trail on every cell, spec, and report
• EU Battery Passport — with our partner KURZ Digital Solutions
• Certification partners for DO 311A, UN 38.3, and beyond