stability chamber for Bulk Drug and Pharmaceutical Manufacturers in Hyderabad
High-precision ICH-compliant stability chambers for Hyderabad's pharmaceutical, API, and bulk drug industry
Our Advanced Solution
Stability Chamber
Hyderabad's pharmaceutical industry runs some of India's most compliance-intensive stability programmes. Kesar Control's stability chambers feature CNC-fabricated SS interiors, illuminated full-view glass doors, and PLC controls with electronic records and audit trail built for the regulatory demands of Genome Valley and IDA pharma clusters.
NABL-traceable calibration and full IQ/OQ/PQ documentation are standard, supporting CDSCO, US FDA, and EU GMP compliance filings. Our service engineers are based locally for rapid AMC response across Hyderabad's major pharma zones.
Our experts will help you select the ideal stability chamber based on your capacity, compliance, and testing requirements.
Our Happy Clients Across Hyderabad

Why Choose Kesar Control?
Excellence in Environmental Testing Solutions
Hyderabad's pharma sector faces the most rigorous regulatory scrutiny in India including routine US FDA inspections. Our 21 CFR Part 11 ready chambers with complete qualification documentation and local service presence keep facilities inspection-ready year-round across Genome Valley, Jeedimetla, and IDA Pashamylaram.
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.
Our PLC chambers provide electronic records, configurable audit trail, batch-wise data reports, and user access controls aligned with 21 CFR Part 11. Combined with NABL-traceable calibration and full IQ/OQ/PQ documentation, they give Hyderabad manufacturers the complete compliance package for US FDA and other international inspections.
Your Requirements, Our Expertise
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