Photostability Chamber for Pharmaceutical Labs in Ankleshwar GIDC
ICH Q1B-compliant photostability testing chambers for export-oriented pharma manufacturers in Ankleshwar's industrial estate
Our Advanced Solution
Photostability Chamber
Ankleshwar GIDC's export-oriented pharma manufacturers require photostability chambers for ICH Q1B light stress testing that meets US FDA and EU GMP regulatory standards. Kesar Control's chambers feature PLC controls with electronic records, audit trail, and calibrated dual lamp systems.
NABL-traceable illuminance and UV calibration with IQ/OQ documentation support CDSCO and international regulatory filings. AMC coverage spans Ankleshwar, Bharuch, and Dahej.
Our experts will help you select the ideal photostability chamber based on your testing requirements and compliance needs.
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Why Choose Kesar Control?
Excellence in Environmental Testing Solutions
Ankleshwar's export pharma manufacturers need photostability chambers with internationally accepted compliance documentation. Kesar Control's PLC-based chambers with 21 CFR Part 11 ready audit trail and electronic records meet US FDA and EU GMP photostability data requirements. Local AMC coverage is available across 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 Photostability Chamber is a specialized environmental chamber that simulates UV and visible light exposure to test the photostability of pharmaceutical formulations, food products, cosmetics, and packaging materials. It helps manufacturers assess stability and shelf life under light conditions.
Kesar Control's Photostability Chambers are designed and built as per ICH Q1B guidelines, which define the standard light exposure requirements for pharmaceutical photostability testing.
The chambers are equipped with both Cool White Fluorescent (CWF) and Near UV lamps to simultaneously expose samples to visible light (≥1.2 million lux hours) and UV light (≥200 Wh/m²) as per ICH Q1B requirements.
Yes. The chambers maintain controlled temperature conditions during light exposure to prevent heat-induced degradation from interfering with photostability test results.
Drug formulations (tablets, capsules, liquids, injectables), APIs, cosmetic products, food items, and primary/secondary packaging materials are commonly tested for light-induced degradation.
Yes. Kesar Control's Photostability Chambers allow the placement of dark (foil-wrapped) control samples alongside exposed samples within the same test run, as required by ICH Q1B guidelines.
Yes. The chamber is built in compliance with GMP requirements and comes with data logging, audit trails, and validation support documentation for regulatory submissions.
The chambers use calibrated lux meters and UV radiometers for real-time monitoring and automatic cutoff once the required light dose is achieved, ensuring repeatable and compliant testing.
Yes. The chamber includes advanced data logging features with USB/Ethernet connectivity, audit trails and supports IQ, OQ, and PQ validation documentation to meet regulatory and compliance requirements.
Kesar Control offers Photostability Chambers in multiple capacities and customizable configurations to suit laboratory-scale research, pilot studies, and large-scale industrial testing requirements.
Yes. Our PLC-based photostability chambers include electronic records, audit trail, and user access controls aligned with 21 CFR Part 11 requirements. Illuminance and UV data are continuously logged with timestamps. Combined with NABL-traceable calibration and IQ/OQ documentation, the full data package supports US FDA regulatory submissions for Ankleshwar pharma manufacturers.
Your Requirements, Our Expertise
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