Regulated Laboratory SolutionsEP / USP Standards

Powder & Tablet Testing Instruments

Precise, pharmacopoeia-compliant physical testing instruments engineered for routine quality control, formulation development, and solid dose characterisation in regulated pharmaceutical and chemical manufacturing.

Flowability & Tapped DensityTablet Hardness & ThicknessDisintegration & FriabilityGranule Characterisation
Pharmacopoeia Compliance

Meets EP 2.9.36, USP <1174>, and USP <1217> standards

Data Integrity Support

Audit trails, secure user roles, and export options

Local Qualification & Service

Full IQ/OQ validation protocols across Ireland and the UK

Precision laboratory powder and tablet testing instrumentation

Professionally Calibrated

Complete traceable qualification packs

Consult
Instrumentation Matrix

Physical Testing Instrumentation Comparison

Side-by-side technical evaluation across powder characterization and solid dosage testing platforms. Technical specifications below are configured for qualification workflows across Ireland and the UK.

Note: Neutral baseline specifications currently marked for technical review and client protocol alignment.
Powder Testing Instruments
Raw material characterization, bulk properties & flow mechanics
Solid State
Pharmacopeial Harmonization:
USP, Ph. Eur., JP & ASTM compliant
Testing ParameterRegulatory StandardTechnical SpecificationStatus
Flowability & Shear TestingASTM D6128 / USP <1174>Shear Cell & Aerated DensityReview
Tapped & Bulk DensityUSP <616> Method I & IIHausner Ratio / Carr IndexReview
Angle of ReposeISO 4324 / Ph. Eur. 2.9.36Dynamic & Static Flow AngleReview
Moisture / Loss on DryingUSP <731> / EP 2.2.32Halogen / IR ThermogravimetricReview
Data Integrity & ComplianceData Integrity & Audit Trail SupportAudit Trail & Electronic SignaturesReview

Standard Qualification Deliverables:

  • Traceable calibration standards
  • IQ/OQ/PQ protocol execution
  • Data integrity and audit trail support
  • Preventative maintenance plan
Tablet Testing Instruments
Finished oral dosage form analysis, physical strength & dissolution
Finished Dose
Pharmacopeial Harmonization:
USP, Ph. Eur., BP & IP standards
Testing ParameterRegulatory StandardTechnical SpecificationStatus
Tablet Hardness & Breaking ForceUSP <1217> / Ph. Eur. 2.9.8Constant Speed / Constant Force (N / kP)Review
Friability & AbrasionUSP <1216> / Ph. Eur. 2.9.7Dual Drum 25 RPM (Automated Discharge)Review
Disintegration TestingUSP <701> / Ph. Eur. 2.9.1Auto-Endpoint Detection BasketReview
Dissolution Testing ProfilesUSP <711> Apparatus 1 & 2Online UV/HPLC Automated SamplingReview
Dimensional MetrologyDigital Contact & Laser MicrometryThickness, Diameter, Length +/-0.01mmReview

Standard Qualification Deliverables:

  • Mechanical calibration tools
  • Temperature & speed verification
  • Software data integrity audit
  • On-site operator certification

Require custom test parameters or method development?

Antech Solutions provides regulatory application support, IQ/OQ qualification protocols, and vendor-certified service across Ireland and the UK.

Application Consultation

Discuss Your Specific Testing Application

Every laboratory workflow has distinct sensitivity, throughput, and regulatory constraints. Share your testing objectives with Antech Solutions, and our technical specialists will recommend the right instrumentation, sampling protocol, and qualification workflow.

Method & Application Feasibility

Evaluate instruments against your target analytes and compliance benchmarks.

Custom Qualification Roadmaps

Tailored IQ/OQ protocols and compliance validation plans for your facility.

Dedicated Technical Specialists

Direct access to senior application chemists across Ireland and the UK.

Speak with a Specialist

Direct review of your analytical requirements

Response within 1 business day
Available for UK & Ireland sites

Confidential assessment tailored to GLP/GMP standards.