ICH PHARMACEUTICAL STABILITY CHAMBERS

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ICH PHARMACEUTICAL STABILITY CHAMBERS
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ICH PHARMACEUTICAL STABILITY CHAMBERS

POL-EKO ICH Stability Chambers provide highly accurate temperature and humidity conditions for pharmaceutical stability testing in accordance with ICH Q1A guidelines. Ideal for long-term, intermediate, and accelerated studies in GMP environments.

(Temperature + Humidity Stability Testing — ICH Q1A)

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Description

POL-EKO ICH Stability Chambers are designed for pharmaceutical R&D, QC laboratories, and manufacturing facilities requiring precise and repeatable temperature–humidity control. These chambers comply with ICH Q1A requirements for long-term, intermediate, and accelerated stability tests of drug substances, finished products, excipients, and packaging materials.

Equipped with the advanced SMART PRO touch controller, the chambers offer precise control, data logging, alarms, and remote monitoring. When paired with LabDesk CFR software, the system meets FDA 21 CFR Part 11 requirements for secure electronic records, audit trails, and controlled access.

Built with acid-resistant stainless steel, forced-air circulation, high-accuracy sensors, and a durable construction, POL-EKO ICH chambers ensure maximum reliability, uniformity, and compliance for pharmaceutical stability programs.

Key Features:

  • Fully supports ICH Q1A stability testing conditions

  • Highly uniform temperature & humidity control

  • SMART PRO 7″ touchscreen controller

  • Remote monitoring: LAN, Wi-Fi, USB

  • Stainless steel chamber (DIN 1.4301)

  • Adjustable / reinforced shelves

  • Over-temperature & sensor alarms

  • 21 CFR Part 11 compliance (via LabDesk CFR)

  • Forced-air circulation for uniformity

  • Double door system with internal glass inspection door

Specifications

  • Temperature Range: 0…+60°C

  • Humidity Range: 10–90% RH

  • Interior: Stainless steel

  • Controller: SMART PRO

  • Connectivity: LAN, Wi-Fi, USB

  • Shelves: 2–4 adjustable

  • Power: 230 V, 50–60 Hz

Applications

  • ICH Q1A stability studies

  • Pharmaceutical product conditioning

  • API and finished dosage form testing

  • Excipient stability

  • Shelf-life determination

  • Packaging compatibility and stability evaluation studies

  • Cosmetics & nutraceutical stability

STANDARDS

ICH

  • ICH Q1A – Stability Testing

  • ICH Q1B – Photostability Testing (dark storage portion)

Pharma / Regulatory

  • FDA 21 CFR Part 11 (via LabDesk CFR software)

  • GMP / GLP workflows

Safety & Performance

  • EN / IEC climate chamber performance standards

Models Available

 

Climatic Chamber KKS 500


CLIMATIC CHAMBER KKS 500

 

Climatic Chamber KKS 700


CLIMATIC CHAMBER KKS 700

 

Climatic Chamber KKS 1200


CLIMATIC CHAMBER KKS 1200

 

Climatic Chamber KKS 1450


CLIMATIC CHAMBER KKS 1450

Accessories & Options

  • Additional shelves

  • Access ports

  • Reinforced trays

  • Door locks

  • Calibration certificates

  • LabDesk CFR software

Additional information

Country

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