stability chamber for Pharmaceutical Manufacturers in Ankleshwar GIDC
ICH and 21 CFR Part 11 ready stability chambers for export-oriented pharma and chemical QC labs in Ankleshwar
Our Advanced Solution
Stability Chamber
Ankleshwar GIDC's pharmaceutical and chemical manufacturers frequently supply export markets, making data integrity a non-negotiable requirement in stability testing. Kesar Control's stability chambers feature SS interiors, full-view glass doors, and PLC controls with electronic records and audit trail.
All units are supplied with NABL-traceable calibration and IQ/OQ documentation accepted by CDSCO and international agencies. Our service team covers Ankleshwar, Bharuch, Dahej, and the Jambusar corridor.
Our experts will help you select the ideal stability chamber based on your capacity, compliance, and testing requirements.
Our Happy Clients Across Ankleshwar

Why Choose Kesar Control?
Excellence in Environmental Testing Solutions
Export-oriented manufacturers in Ankleshwar need stability data that satisfies both Indian and international regulators. Our 21 CFR Part 11 ready PLC systems with audit trail and electronic records meet US FDA and EU GMP expectations. Dedicated AMC support is available across Ankleshwar and Bharuch district.
Superior Quality & Precision Engineering
Compliance with Global Industry Standards
Reliable Customer Support & Custom Solutions
Technical Specification
| Temperature Range | 20 ℃ to 60 ℃ |
|---|---|
| Humidity Range | 40%RH to 95%RH |
| Accuracy | ±0.2 ℃ & ±2.0% RH |
| Uniformity | ±2.0 ℃ & ±3.0% RH |
| Test Suitable For | 25 ℃ & 60% RH, 30 ℃ & 65% RH 40 ℃ & 75% RH, 30 ℃ & 75% RH |
| Specially designed chambers for Low Humidity conditions such as 25 ℃ 40% RH, 40 ℃ 25% RH, 30 ℃ 35% RH | |
| Control System | PLC or PID Based |
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FAQ'S
A stability chamber is a laboratory device that replicates controlled environmental conditions, specifically temperature and relative humidity, to test the shelf life, degradation, and stability of pharmaceuticals, chemicals, food products, and cosmetics.
Kesar Control Stability Chambers support all standard ICH Q1A conditions: 25°C/60% RH, 30°C/65% RH, 40°C/75% RH, and special low-humidity conditions such as 30°C/75% RH.
A standard stability chamber is a reach-in unit suitable for smaller batch testing, while a walk-in stability chamber is a room-sized version that allows scientists to physically walk in, ideal for large-scale pharmaceutical stability studies.
Kesar Control Stability Chambers offer temperature accuracy of ±0.2°C and humidity accuracy of ±2.0% RH, with uniformity of ±2.0°C and ±3.0% RH.
Yes. The chambers feature automated data logging with audit trails, alarm systems, and software compatible with 21 CFR Part 11 requirements for pharmaceutical regulatory submissions.
Yes. Kesar Control offers specially designed chambers for low-humidity stability testing, such as 25°C/60% RH, 40°C/75% RH, and 30°C/65% RH conditions.
With regular maintenance and calibration through Kesar Control's AMC services, a stability chamber can operate reliably for 10–15 years or more.
Stability chambers are used in pharmaceuticals, APIs, nutraceuticals, cosmetics, food & beverages, biotechnology, and chemical industries for regulatory stability testing.
Kesar Control Stability Chambers are equipped with safety alarms for temperature and humidity deviations, compressor overload protection, low water level alerts, sensor failure indications, and automatic system cutoffs to protect valuable samples.
Yes. Kesar Control offers customized Stability Chambers with different capacities, shelving arrangements, access ports, monitoring systems, and operating ranges to meet specific testing and laboratory needs.
Yes. Our PLC-based chambers include electronic records, audit trail, user authentication, and configurable access controls aligned with 21 CFR Part 11 requirements, making them suitable for US FDA-regulated stability dossiers from Ankleshwar's export pharma manufacturers.
Your Requirements, Our Expertise
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