stability chamber for Pharmaceutical Manufacturers in Nadiad
ICH Q1A-compliant stability chambers for formulation companies and API producers in Nadiad and Kheda district
Our Advanced Solution
Stability Chamber
Nadiad's pharmaceutical manufacturers preparing domestic and export stability dossiers need chambers with reliable ICH performance and strong documentation. Kesar Control's stability chambers feature CNC-fabricated SS interiors, full-view glass doors, and PLC controls with electronic records and audit trail.
NABL-traceable calibration and IQ/OQ documentation are provided for CDSCO and WHO-GMP filings. Our service network covers Nadiad, Kheda, Anand, and the central Gujarat pharma corridor.
Our experts will help you select the ideal stability chamber based on your capacity, compliance, and testing requirements.
Our Happy Clients Across Nadiad

Why Choose Kesar Control?
Excellence in Environmental Testing Solutions
Nadiad's pharma units prepare stability dossiers for both CDSCO and export market submissions. Kesar Control's PLC chambers with electronic audit trail and complete qualification documentation meet both domestic and international filing requirements. Local AMC coverage across the central Gujarat pharma belt ensures ongoing support.
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 |
Explore Our Range
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.
The STD model has an SS 304 interior with GI powder-coated exterior, suitable for standard industrial QC. The GMP model has SS 304 interior and SS 304 exterior, meeting GMP facility standards. The CGMP model has SS 316 interior and SS 304 exterior, designed for the strictest GMP and cGMP compliance requirements. Most Nadiad pharma manufacturers choose the GMP or CGMP model for regulatory submissions.
Your Requirements, Our Expertise
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