Pharmaceutical Division

Pharmaceutical

Innovation and excellence in top-tier pharmaceutical testing equipment and related services for QC, R&D and production environments.

USP · EP · JP · ICH 21 CFR Part 11 GMP Compliant
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USP / EP / JP compliant All instruments meet or exceed pharmacopoeia requirements.
description
21 CFR Part 11 ready Full audit trail and data integrity support built in.
biotech
IQ/OQ/PQ support Complete installation and operational qualification documentation.
Pharmaceutical by the numbers
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USP · EP · JP
Pharmacopoeia Compliant
All major global pharmacopoeias supported.
description
21 CFR Part 11
Data Integrity
Full audit trail, electronic signatures, access control.
biotech
ICH Q1A
Stability Tested
Stability chambers compliant with ICH guidelines.
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IQ/OQ/PQ
Qualification
Full qualification documentation and on-site services.
Precision instruments for pharmaceutical QC and R&D
GMP
Compliant
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Every measurement is audit-defensible. Every software action is traceable.

Pharmaceutical Testing

Precision instruments for pharmaceutical QC and R&D

Torontech's Pharmaceutical division delivers innovation and excellence in top-tier pharmaceutical testing equipment. Our instruments are designed for laboratories that demand accuracy, compliance and reliability.

Why pharmaceutical labs choose us
  • check_circleFull USP, EP, JP and ICH method coverage
  • check_circle21 CFR Part 11 software ready out-of-box
  • check_circleIQ/OQ/PQ documentation included
  • check_circleCalibration with full uncertainty statements
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Product Categories

Complete pharmaceutical testing solutions

Comprehensive instrumentation for every stage of pharmaceutical quality control.

science

Dissolution Testers

USP-compliant dissolution testing systems with automated sampling.

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Disintegration Testers

Tablet and capsule disintegration analysis per pharmacopoeia methods.

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Hardness Testers

Tablet hardness, thickness and friability testing instruments.

thermostat

Stability Chambers

ICH-compliant stability testing with precise temperature and humidity control.

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Melting Point Apparatus

Automated melting point determination for API and excipient characterization.

analytics

Data Management

21 CFR Part 11 compliant software with audit trails and electronic signatures.

Compliance

Built for regulated pharmaceutical environments

Our instruments are designed to meet the most stringent pharmaceutical regulatory requirements worldwide.

USP United States Pharmacopeia compliance for dissolution, disintegration and hardness testing.
EP European Pharmacopoeia alignment for all applicable test methods.
21 CFR Part 11 Electronic records and signatures compliance with full audit trail support.
ICH Q1A Stability testing guidelines for new drug substances and products.
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When regulators review your data, our work is on the line. We take that seriously.
Torontech Pharma DivisionOur standard
Services

Complete lifecycle support

  • Installation & IQ/OQ/PQ — Professional on-site installation with full qualification documentation
  • Preventive Maintenance — Scheduled maintenance contracts to ensure continuous compliance
  • Calibration & Validation — NIST-traceable calibration with full certificates
  • Operator Training — Comprehensive training programs for laboratory staff
Pharmaceutical Solutions

Equip your laboratory with confidence

Contact our pharmaceutical specialists to discuss your QC and R&D instrumentation needs.

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