Local application and service support across Ireland and the UK.
Analytical Feasibility Studies & Method Viability
Evaluate system compatibility, sensitivity limits, and measurement precision on your exact materials before you purchase. We assess real samples in our specialised laboratory facilities across Ireland and the UK.
De-risk Investment
Validate analytical feasibility before committing capital expenditure.
Real-Sample Testing
Trial actual formulation matrices in controlled laboratory environments.
Comprehensive Reporting
Receive full method viability, LOD/LOQ, and regulatory compatibility data.
Standard Protocol
Confidential Trial Roadmap
100%
Confidentiality & Data Integrity
2-3 Wks
Average Study Turnaround
GMP / GLP
Compliance Ready
What is Covered in a Feasibility Study
Eliminate implementation risks before investing. Our structured feasibility studies evaluate your samples, testing environments, and regulatory requirements to establish clear technical proof of concept.
Evaluation of raw materials, blends, or active ingredients. We test spectral responses, signal-to-noise ratios, and assess matrix interference across your specific sample types.
- Spectral library viability analysis
- Optical penetration depth assessment
- Interference and moisture baseline checks
Determination of the most effective analytical hardware, probe geometry, laser wavelengths, or NIR/Raman sensors tailored to your benchtop or in-line production environment.
- Optimal probe and flow-cell geometry
- Sensor sensitivity and scan-rate specs
- Atmospheric and ATEX classification review
Executing real matrix measurements to prove repeatability, linearity, limit of detection, and measurement speed before committing capital expenditure.
- Repeatability and calibration models
- Limit of Detection (LOD) verification
- Comparative reference testing against HPLC/Karl Fischer
Assessment of data connectivity, automation requirements, and seamless integration into existing DCS, SCADA, or laboratory information management systems (LIMS).
- OPC-UA and industrial bus mapping
- Automated batch release trigger feasibility
- Real-time feedback loop verification
Gap analysis for data integrity compliance, electronic audit trails, and validation requirements tailored to HPRA, MHRA, and FDA standards.
- User Requirement Specification (URS) alignment
- IQ/OQ/PQ validation protocol outlines
- Data integrity risk matrix
A complete dossier containing all experimental data, instrument recommendations, payback timelines, and an actionable step-by-step implementation strategy.
- Comprehensive data dossier with raw spectra
- Capex and operational payback projections
- Turnkey deployment schedule and milestones
Ready to evaluate your process or lab samples?
Speak directly with an application specialist in Ireland or the UK to discuss sample requirements, confidentiality agreements, and timelines.
Study Methodology & Expected Outputs
Our structured study framework ensures every analytical solution is verified, robust, and aligned with regulated laboratory and manufacturing requirements across Ireland and the UK.
4-Stage Method Development Lifecycle
Definition of analytical targets, critical quality attributes (CQAs), sample matrix assessment, and regulatory compliance requirements.
Multi-parameter test runs across temperature, matrix variations, and spectral ranges to establish optimal measurement windows and signal stability.
Stress testing method parameters, determining limits of detection (LOD/LOQ), repeatability verification, and transferability under production settings.
Multivariate regression analysis, spectral preprocessing, calibration set cross-validation, and outlier detection algorithm validation.
Expected Project Deliverables
Every completed study concludes with actionable documentation, calibrated models, and full compliance qualification.
Analytical Feasibility Report
Complete validation metrics
Comprehensive quantitative data package with raw spectral records, precision studies, and instrument qualification logs.
Standard Operating Procedures (SOP)
Ready-to-deploy protocols
Step-by-step instrument operation, sample preparation, diagnostic checks, and maintenance documentation.
Calibrated Predictive Models
Transferable model files
Exportable chemometric models compatible with standard process analytical technology (PAT) management software.
Regulatory Compliance Dossier
Audit-ready evidence
Complete trace matrices supporting analytical quality standards, data integrity requirements, and pharmacopoeial guidelines.
Need a custom study protocol for your facility?
Speak with our application specialists to define custom testing parameters and sample feasibility.
Request a Feasibility Study Quote
Connect directly with Antech Solutions. Share your analytical instrument or process specifications to receive an accurate feasibility proposal and project estimate.
Tailored Feasibility Assessment
In-depth technical review matched to your laboratory or production workflow.
Fast 24-48h Response
Direct evaluation from our analytical specialists across Ireland and the UK.
Regulated Compliance Assurance
Protocol-aligned methodology meeting strict GMP, GLP, and ISO standards.
Direct Laboratory Enquiries
Covering regulated laboratories and manufacturing facilities across Ireland and the United Kingdom.
Contact Us – Antech Solutions
Complete the details below and our team will prepare your feasibility study quote.