GammabrauKnowledge

Learn thescience.

Why gamma, how it compares, and short guides for QA, regulatory and packaging teams.

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(01) Why gamma

Clean, without compromise.

Penetration

All the way through.

Dense and palletised goods are treated uniformly, inside sealed packaging.

Temperature

A cold process.

Negligible heat rise — safe for plastics, drugs and spices.

Residue

Nothing left behind.

Unlike EtO, there is no gas to aerate. Products ship immediately.

Safety

Never radioactive.

Gamma processing does not make products radioactive. Safe to handle and consume.

(02) Choosing a method

Gamma, compared.

How Cobalt-60 gamma stacks up against the other industrial sterilization methods.

GammaAvailable hereElectron beamX-rayEthylene oxide
PenetrationHigh — full pallets and dense goodsLimited — low-density cartonsHighDepends on gas diffusion
Cycle timeHoursSeconds to minutesHoursDays, including aeration
ResidueNoneNoneNoneEO residuals, needs aeration
TemperatureAmbient, cold processSlight riseAmbientHeat and humidity
PackagingAny sealed packagingAny sealed packagingAny sealed packagingMust be gas-permeable
ReleaseDosimetric releaseDosimetric releaseDosimetric releaseOften biological indicators
(03) Knowledge

Guides and glossary.

Short guides for QA, regulatory and packaging teams.

Guide · 2 minWhat a kilogray actually means

One gray is one joule of energy absorbed per kilogram of product; a kilogray (kGy) is a thousand of those. Sprout inhibition needs a fraction of a kGy, spice decontamination around 6–14 kGy, and medical device sterilization typically 25 kGy or a validated lower dose.

Guide · 3 minVDmax25 vs Method 1

Both are ISO 11137-2 methods to set a sterilization dose. VDmax25 substantiates 25 kGy using a small verification test and suits low bioburden products. Method 1 derives a product-specific dose from bioburden data and can allow a lower dose for sensitive materials.

Guide · 2 minWhy dose audits matter

Bioburden can drift as suppliers, materials or processes change. Periodic dose audits confirm the established dose still delivers the required sterility assurance level, keeping your validation current.

Guide · 2 minPacking cartons for gamma

Uniform density and a consistent loading pattern give a tight dose uniformity ratio (Dmax / Dmin). Keep the validated carton size, product count and orientation the same for every batch.

Guide · 2 minReading your certificate

Check that the delivered minimum dose is at or above your required minimum, and the delivered maximum is at or below your maximum acceptable dose. Batch numbers and box serials link the certificate to the goods received.

SAL
Sterility assurance level — probability of a non-sterile unit, typically 10⁻⁶.
Bioburden
The population of viable microorganisms on a product before sterilization.
Dmin / Dmax
Lowest and highest dose measured within a processed load.
DUR
Dose uniformity ratio — Dmax divided by Dmin.
Dosimeter
A calibrated device that measures absorbed dose in the product.
IQ / OQ / PQ
Installation, operational and performance qualification of the process.
(04) FAQ

Common questions.

Will irradiation make my product radioactive?

No. Gamma rays from Cobalt-60 do not have enough energy to make materials radioactive. Treated products are safe to handle, sell and consume immediately.

Do products need to be unpacked?

No. Gamma rays pass through cardboard, plastic, glass and foil, so products are treated in their final sealed cartons.

Does it affect the taste or colour of spices?

At approved doses there is no meaningful change in flavour, aroma or colour — which is why it is widely used for export-grade spices.

How long does processing take?

It depends on the dose and volume of your consignment. Call or WhatsApp us with product details and we will confirm a schedule.

Can you support validation for a new product?

Yes. We support dose mapping and validation studies, working with your QA team or testing laboratory on sterility and bioburden testing.

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