Hygienic conveying
CIP-ready hygienic conveying with validated cleaning cycles and no dismantling to clean.
- Cleanroom-compatible handling
Pharmaceutical & Life Sciences
Equipment that holds up to the audit as well as the process.
We design, manufacture, install, automate, integrate and maintain process, conveyance and end-of-line equipment for pharmaceutical and life science production.
In a GMP environment the specification is only half the job – the other half is the paperwork that proves the specification was met, and the discipline to work inside a validated area without compromising it.
- Food-safe contact surfaces, crevice-free welds
- Traceable materials dossier and weld logs
- DQ, IQ, OQ and PQ support
- CE certified machinery
What we deliver on pharma sites.
Bespoke rather than catalogue: equipment specified around your product flow, cleaning cycle and the footprint you actually have.
IBC washing systems
Automated wash, vacuum dry, pressure test and certification, with validation labelling in cycle.
- CE certified, built in Kilkenny
Capacity & flow analysis
Capacity planning, bottleneck analysis and process flow studies before capital is committed.
- Layout drawings supplied
Robotic handling & vision
Precision handling, assembly and inspection cells for controlled environments.
- Traceability data captured
Qualification support
Design, installation, operational and process qualification on greenfield and brownfield work.
- Documentation packs supplied
Planned maintenance
SLA cover with held critical spares, KPI reporting and digital service logs.
- Fitter secondment available
Compliance is designed in, not added later.
We have a track record delivering on FDA-regulated sites and inside validated suites, to the standards your quality team works from.
- EU GMP Annex 1Hygienic design aligned to sterile manufacturing requirements.
- FDA-regulated sitesExperience working inside FDA-regulated pharmaceutical production.
- ISO 9001 and ISO 14001Delivery on sites operating to quality and environmental management standards.
- Materials traceabilityCerts, weld logs and finish records handed over as a dossier.
- Machine safetyRisk assessment, guarding and CE certification on machinery we supply.
- GMP-trained teamsEngineers inducted and experienced in validated environments.
Working on live sites
Installing inside a validated area.
We 3D scan the space, design around the available footprint and cleaning access, and plan works around your shutdown window – method statements and risk assessments agreed before anyone arrives.
Factory acceptance testing happens in Kilkenny so site time is installation and commissioning, not fabrication.
- 3D site scanning and dimensional survey
- FAT before anything ships
- IQ/OQ support and handover training
- Works sequenced around production
Pharma projects - common questions.
Can you work inside a validated suite?
Yes. Works are planned around your shutdown window with method statements and risk assessments agreed up front, and we support IQ and OQ with the documentation pack.
What documentation do we get?
A traceable materials dossier, weld logs, FAT records and a validation pack, plus CE certification on machinery.
Do you support qualification?
We support DQ, IQ, OQ and PQ on both greenfield and brownfield projects, with over three decades of qualification experience on regulated sites.
Who maintains it afterwards?
Our maintenance unit, under an SLA with held critical spares, KPI reporting and the option of fitters seconded into your team.
