Walk in stability chamber for Bulk Drug and API Manufacturers in Hyderabad
High-capacity ICH-compliant walk-in chambers for Hyderabad's pharmaceutical, API, and bulk drug manufacturing industry
Our Advanced Solution
Walk In Stability Chamber
Hyderabad is India's pharmaceutical capital in terms of bulk drug and API output, with hundreds of manufacturers across Genome Valley, Jeedimetla, and IDA Pashamylaram running complex stability programmes for domestic and global markets.walk-in stability chambers are standard equipment for large pharma operations here, enabling simultaneous testing of multiple product batches under ICH-defined conditions. Kesar Control's chambers are built at the scale and precision that Hyderabad's pharmaceutical industry demands.
Built with modular PUF-insulated panels for on-site assembly, water and vapor-tight SS interiors, and PLC-based control with electronic audit trail, these chambers are designed for the regulatory intensity that Hyderabad's export-focused pharma sector operates under. Multi-pane vacuum-sealed observation windows allow non-intrusive monitoring, and heavy-duty electro-polished SS trays handle large sample loads across years-long test cycles. NABL-traceable calibration and full IQ/OQ/PQ documentation are standard, supporting filings for CDSCO, US FDA, and EU GMP compliance.
Our experts will help you select the ideal walk in stability chamber based on your capacity, compliance, and testing needs.
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, with US FDA inspections common across Genome Valley and IDA clusters. Kesar Control's walk-in chambers deliver 21 CFR Part 11 ready data systems, complete qualification documentation, and chambers built to withstand years of continuous operation without calibration drift. Our service engineers are based locally for rapid response across Hyderabad's major pharma zones.
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 Walk-In Stability Chamber is a large-scale environmental testing room that a scientist can physically enter to perform stability studies. It is used to test pharmaceutical products, vaccines, and chemicals simultaneously under controlled temperature and humidity conditions.
Kesar Control's Walk-In Stability Chambers support all major ICH Q1A stability testing conditions including 25°C/60% RH (Long Term), 30°C/65% RH (Intermediate), 40°C/75% RH (Accelerated), and 30°C/75% RH.
The interior is made of high-quality stainless steel with ready-made PUF panel construction, ensuring hygiene, durability, and consistent temperature distribution throughout the chamber space.
The chambers feature advanced air circulation systems and precision sensors to maintain uniformity of ±2.0°C temperature and ±3.0% RH across the entire chamber volume, even under heavy load.
Yes. Kesar Control's Walk-In Stability Chambers are equipped with multi-pane vacuum-sealed observation glass windows, allowing visual inspection of samples without disturbing the test conditions or compromising human safety.
The chambers use PLC and HMI-based control systems with real-time data logging, remote monitoring capabilities, and 21 CFR Part-11 compliant software features.
Walk-In Stability Chambers are available in a wide range of capacities, starting from 2400 liters to 24000 liters, fully customizable based on batch sizes and testing requirements.
Yes. Kesar Control provides complete installation, IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) documentation support as part of their service offering.
The chamber is equipped with safety alarms for temperature and humidity deviations, emergency door release systems, overload protection, and sensor failure alerts to ensure operator safety and sample protection.
Yes. Kesar Control offers fully customized Walk-In Stability Chambers with configurable dimensions, shelving systems, access doors, lighting, monitoring systems, and temperature/humidity ranges based on specific industry and testing needs.
Our PLC-based chambers provide electronic records, configurable audit trail, user access controls, and batch-wise data reports that align with 21 CFR Part 11 requirements. Combined with full IQ/OQ/PQ qualification documentation and NABL-traceable calibration, our chambers give Hyderabad pharma manufacturers the complete documentation package needed to remain inspection-ready for US FDA and other international regulatory agencies.
Your Requirements, Our Expertise
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