ATEX in the Pharmaceutical Industry
ATEX · IECEx · Pharma

ATEX in the Pharmaceutical Industry

Independent ATEX pharmaceutical industry support — hazardous area classification, EPD and Ex inspection to IEC 60079-17 for solvent processes and combustible powders, from API and coating to tableting and packaging.

Cleanroom reactor in a pharmaceutical facility (ATEX)
IEC 60079-17inspection standard
CompExcertified inspector
25+ yearsindustrial Ex experience
Gas + dustsolvents & powders
The risk

Two risks at once: vapour and dust

Pharmaceutical processes combine flammable solvent vapour (reaction, coating, cleaning) with combustible powders (milling, blending, tableting, dust collection). Both can form explosive atmospheres, so classification and inspection have to address gas and dust together.

Scope

What I check in pharma plants

Gas & dust zones

Solvent areas and dust-handling equipment — classification for both gas and dust.

Ex equipment

Reactors, dryers, mills, dust collectors and their Ex equipment to IEC 60079-17.

EPD & controls

Earthing, static control and a current EPD that matches the process.

Cleanroom reactor in a pharmaceutical facility (ATEX)
Tableting and packaging line in a pharmaceutical plant (ATEX)

Request a pharma ATEX quote

Tell me the solvents and powders involved and any existing classification/EPD. I will advise whether a gas, dust or combined scope fits, and provide a quote.

Independent CompEx certified inspection and explosion protection support. Final scope and fee are agreed individually. Email: info@atexfullcare.com.

FAQ

Frequently asked questions

Do you handle dust as well as solvents?

Yes — combustible dust (Zones 20/21/22) and solvent vapour (Zones 0/1/2) are assessed together where both are present.

Can this support GMP and audits?

The ATEX classification, EPD and inspection provide the explosion-safety evidence that sits alongside your quality and audit requirements.

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