Local application and service support across Ireland and the UK.
Analytical Technology & Lifecycle Support for Regulated Pharma
Application-led analytical instrumentation, complete qualification protocols, and ongoing lifecycle support for regulated laboratories and manufacturing teams across Ireland and the UK.
Validated for stringently regulated environments
Full data integrity compliance across all workflows
Rigorous analytical instrument validation protocols
Real-time in-line quality assurance and control
Analytical tools engineered for regulated pharmaceutical production
We supply qualified testing instrumentation, Process Analytical Technology (PAT), and validation lifecycle support across Ireland and the UK.
Core Applications
Industry Challenges & Solutions
Regulatory Requirements
Constantly evolving Annex 11 and FDA requirements demand end-to-end trace logs and validated analytical methods.
Analytical Testing
High-throughput laboratory queues face sample backlogs, solvent waste, and operator-to-operator variance.
Process Validation
Transferring batch formulations into commercial manufacturing risks blend inconsistency and drying endpoint drift.
Need guidance for a specific regulated test method?
Talk to our application specialists for system recommendations and on-site demonstrations.
Real-time process intelligence for regulated manufacturing
Move from retrospective batch testing to continuous quality assurance. Our PAT solutions integrate robust optical sensors, sample interfaces, and chemometric algorithms directly into manufacturing lines across Ireland and the UK.
In-line and On-line Process Spectroscopy
Eliminate sampling latency and prevent off-spec batches. Our fiber-optic Raman, NIR, and UV-Vis systems monitor critical process parameters (CPPs) and critical quality attributes (CQAs) directly inside reactors, fluid beds, and extruders without taking physical samples offline.
Core PAT Technologies
Engineered for pharmaceutical, biopharmaceutical, and fine chemical production environments.
Compliance-First Validation and Deployment
PAT projects require more than hardware. Antech Solutions provides comprehensive method development, chemometric calibration transfer, and complete GAMP-aligned qualification to satisfy FDA and HPRA regulatory requirements.
Targeted PAT Implementations
Drying Endpoint Determination
Eliminate over-drying and batch variations with continuous moisture tracking in fluid bed dryers and vacuum ovens.
Real-Time Blend Uniformity
Wireless spectrophotometric sensors in rotating blenders providing instantaneous homogeneity verification without sample thief bias.
Raw Material Identification
Handheld and benchtop Raman/NIR systems for container identification and raw material verification at warehouse intake.
Need a bespoke PAT feasibility study?
Send your formulation samples or process parameters to our laboratory team in Ireland for method evaluation and proof-of-concept testing.
Technical services built for regulated science
From equipment qualification and method deployment to long-term operational maintenance, we deliver support across Ireland and the UK.
Need custom protocol development or multi-site maintenance?
Our application specialists provide customized validation packages tailored to your SOPs.
Ready to elevate your laboratory compliance and analytical efficiency?
Partner with Antech Solutions for application-led analytical technology, equipment qualification, and ongoing support across Ireland and the UK.
Have a pressing qualification or maintenance question? Speak directly with our engineering team today.