Pharmaceutical Quality Control & Testing

Precision Tablet Testing Built for Pharmacopeial Monographs

Stricter monographs and data integrity requirements demand faster testing without sacrificing analyst workload.

  • Aligned with USP / EP / JP monograph testing methods
  • Data Integrity focused
  • Full IQ/OQ qualification protocols
Precision laboratory tablet testing system for dissolution and hardness measurement
EP / USP Referenced Methods

Automated Reports

Audit Trail Ready

Multi-Parameter

Hardness & Disintegration

Regulated Lab Operations

Balancing Stringent Compliance with Laboratory Throughput

Regulated laboratories face constant friction between the need for speed and the absolute requirement for uncompromised compliance. We deliver the analytical technology, qualification protocols, and lifecycle support needed to achieve both.

Pre-configured IQ/OQ/PQ protocols tailored to your QA standards
Automated instrumentation cutting sample cycle time by up to 40%
Unified data management ensuring complete audit-trail traceability
Pharmacopeial Evolution

USP, EP & JP Alignment

High Regulatory Impact

Rapidly changing compendial standards require constant method re-validation, instrument requalification, and heightened audit readiness.

Workflow Bottlenecks

Sample Backlogs & Turnaround Time

Operational Risk

Manual sample preparation, multi-step analytical sequences, and legacy instrument downtime slow critical batch release cycles.

Data Integrity & Verification

Audit Trails & Data Integrity

Compliance Priority

Unbroken electronic audit trails, automated metadata capture, and human-error elimination are required for every run.

Core Testing Capabilities

Standard-Compliant Physical & Analytical Testing Systems

Supporting regulated laboratories and pharmaceutical manufacturing teams across Ireland and the UK with qualified physical testing instrumentation.

Formulation & QC
Dissolution Testing
Precision systems for automated and manual dissolution profiling to evaluate active ingredient release rates across standard and specialized dosage forms.

Key Capabilities

  • Apparatus 1, 2, and specialized vessel formats
  • Automated sampling and online UV/HPLC integration
  • Pharmacopeial qualification and bath temperature monitoring
Solid Dosage QC
Disintegration Testing
Reliable disintegration systems verifying breakdown times of tablets and capsules under strictly regulated temperature and agitation conditions.

Key Capabilities

  • Automated endpoint detection and individual basket timers
  • EP, USP, and JP compliance standard protocols
  • Ergonomic quick-clean bath and modular test stations
Physical Testing
Hardness & Physical Characterization
Multi-parameter physical testing instrumentation measuring tablet hardness, diameter, thickness, and weight with high repeatable accuracy.

Key Capabilities

  • Multi-parameter measuring jaws with linear force profiles
  • Integrated weighing balances and optical thickness sensors
  • Data export for electronic batch records
Physical Testing Portfolio

Copley Scientific Instrumentation

Explore primary instrumentation categories for routine quality control, galenical development, and regulatory batch release.

Laboratory dissolution testing bath apparatus
EP / USP Compliant

Pharmacopeial Solid Dosage Testing

Dissolution Testers
Reliable bath and bathless systems engineered for precise release rate profiling and compliance with EP, USP, and JP standards.
Vessel temperature monitoring, qualification tools, automated sampling ready
Automated basket disintegration testing device
Batch Validation

Dosage Breakup & Time Verification

Disintegration Testers
Robust single and multiple basket disintegration testers delivering repeatable cycle control and clear basket visibility during runtime.
Independent station timing, quick-release basket assemblies, digital heating baths
Precision tablet hardness and diameter testing instrument
Multi-Parameter

Physical Dimensions & Breaking Force

Tablet Hardness & Combination Testers
Accurate testing systems assessing breaking force, diameter, thickness, and weight to ensure structural integrity across production batches.
Constant speed & force modes, debris collection trays, printer and LIMS export
Pharmaceutical friability drum and tap density test unit
Physical Characterisation

Mechanical Durability & Powder Compaction

Friability & Tap Density Testers
Standardised drum rotation and graduated cylinder tapping systems for determining tablet attrition and settled powder packing characteristics.
Automated drum discharge, single and dual station options, calibrated drop heights
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Analytical & Compliance Services

Application-led testing and lifecycle support

Supporting regulated laboratories and manufacturing teams across Ireland and the UK with reliable instrumentation, method validation, and quality oversight.

QC & Release
Batch Release Testing
Comprehensive analytical verification of raw materials, in-process samples, and finished pharmaceutical batches conforming to strict specifications.
ICH Guidelines
Stability & Formulation Studies
Accelerated and real-time environmental chamber testing to monitor shelf-life integrity, degradation pathways, and container closure systems.
EP / USP / BP
Pharmacopeial Compliance Audits
Method verification and laboratory audit readiness assessments ensuring full adherence to current European, United States, and British pharmacopeias.
Manufacturing QA
In-Process Quality Checks
Rapid turnaround testing protocols and instrumentation monitoring to ensure operational continuity throughout active production cycles.

Require bespoke validation or qualification protocols?

Our analytical technical specialists can assist your quality assurance team.

Talk to a Specialist
Engineering & Compliance

Technical Services & Validation Support

Application-led analytical technology, qualification, and lifecycle support engineered for regulated laboratories and manufacturing teams.

Application Support
01

Method Setup & Optimization

Chromatography, spectroscopy, and dissolution method deployment

Direct technical support from senior analytical specialists to streamline assay validation, transfer protocols, and minimize instrument run times while maintaining data integrity.

Compliance & Validation
02

IQ/OQ Qualification & Calibration Support

GxP compliance, traceable standards, and audit-ready documentation

IQ/OQ qualification protocol support and documentation tailored for regulated pharmaceutical, biopharma, and medical device laboratories across Ireland and the UK.

Lifecycle Care
03

Preventative Maintenance & Technical Service Agreements

Scheduled servicing, rapid diagnostics, and OEM-grade spare parts

Structured service level agreements designed to prevent unplanned instrument downtime, ensure optical and mechanical precision, and maximize laboratory throughput.

Regulated Laboratory Compliance

Our service protocols are developed with reference to MHRA, HPRA, FDA, and European Pharmacopoeia regulatory expectations. We deliver complete, defendable documentation packages with every calibration and validation engagement.

Fully traceable calibration tools conforming to ISO/IEC 17025 standards
Direct engineering support across Ireland and UK manufacturing hubs
Emergency response options with certified OEM replacement parts
Comprehensive validation binders ready for immediate regulatory inspection
Rapid dispatch SLA available
Ireland & UK Coverage

Need a dedicated service agreement?

Speak directly with an analytical service specialist.

Complete Laboratory Solutions

Explore Complementary Offerings

Support every stage of your analytical workflow across Ireland and the UK with integrated instrumentation supply and certified technical services.

Analytical laboratory instrumentation and chromatography equipment
Equipment & Hardware
Related Products
Precision instrumentation, dissolution systems, chromatography consumables, and analytical technologies tailored for regulated laboratories.
  • Dissolution, HPLC, and spectroscopic analytical systems
  • Manufacturer-certified parts and compliant consumables
  • Fully documented supply chain and traceability specs
Service engineer calibrating laboratory equipment
Lifecycle & Compliance
Related Services
Comprehensive qualification, proactive preventative maintenance, calibration, and emergency repair delivered by factory-trained field engineers.
  • IQ/OQ/PQ protocol execution and audit readiness
  • Preventative maintenance plans and emergency repairs
  • ISO-traceable multi-vendor calibration programs
Regulated laboratory and pharmaceutical production facility
Tailored Compliance
Sector Expertise

Related Industries

Antech Solutions delivers analytical technology, qualification, and lifecycle support engineered to satisfy strict regulatory requirements across Ireland and the UK.

Pharmaceutical & Biopharma
Regulated Manufacturing
Quality Assurance & QC Testing
Life Sciences & Research Labs
Compliant with GMP, GLP & ISO standards
Explore all industries

Application Ecosystem

Related Solution Hubs

Explore analytical instruments, qualification workflows, and dedicated methodologies tailored to regulated laboratory and production environments.

Powder Testing
Characterise powder flowability, bulk density, and compressibility for formulation and manufacturing consistency.
Process Analytical Technology
Enable real-time inline and online monitoring of critical quality attributes during active synthesis and blending.
Raw Material Identification
Verify incoming raw material identity rapidly through container packaging with non-destructive handheld spectroscopy.
Safety and Security
Rapidly identify unknown narcotics, hazardous chemicals, and explosives with ruggedised field-ready analysers.
Knowledge Hub

Latest Insights and Technical Resources

Explore recent application notes, analytical methodologies, regulatory updates, and technical insights from our specialists.

Optimize Your Tablet Testing Workflow Today

Connect with our technical specialists to evaluate your laboratory testing requirements, streamline qualification, and enhance testing compliance.

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Additional product coverage

This section adds product and application coverage carried across from the previous Antech website so visitors can find the right family from this live page.

Accessories for Tablet Dissolution Testing | Available form Antech

Add clearer tablet dissolution/disintegration accessories coverage: vessels, baskets, paddles, sinkers, consumables and accessory support around the existing tablet testing family.

Additional product coverage

This section completes another migrated product coverage pass from the previous Antech website so visitors can reach the correct live product family more easily.

Tablet Analysis – cGMP Handheld Raman NIR Spectrometers

Add tablet analysis bridge coverage connecting tablet testing, dissolution, disintegration, hardness and friability workflows.