China Environmental Test Chambers manufacturer
Dongguan Precision Test Equipment Co., Ltd.
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Pharmaceutical Stability Testing Chamber OEM ODM For Cold Storage

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Dongguan Precision Test Equipment Co., Ltd.

City: guangzhou

Country/Region:china

Tel:86-0769-8701-1382

Contact Person:
Mr.Precision
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Pharmaceutical Stability Testing Chamber OEM ODM For Cold Storage

Brand Name PRECISION
Model Number RTH-270
Certification ISO
Place of Origin CHINA
Minimum Order Quantity 1
Price $6000
Payment Terms T/T
Supply Ability 100/month
Delivery Time 15 working days
Packaging Details Standard export packaging
Customized support OEM ODM
Origin China
Material Stainless Steel
Controller Programmable LCD Touch Screen
Temp accuracy: 0.5°C
Temp uniformity 0.5°C
Refrigerant Environmental friendly R23/R404
Detailed Product Description

Energy-saving Stability Testing Chamber for Pharmaceutical Testing and Cold Storage

In the pharmaceutical realm, where product integrity and efficacy are non-negotiable, the Energy-saving Stability Testing Chamber emerges as a vital asset. This chamber is specifically engineered to address the unique demands of pharmaceutical testing and cold storage, ensuring that medications maintain their potency and quality throughout their shelf life.

1. Product Name and Purpose

 
This advanced chamber is dedicated to simulating a wide range of temperature and humidity conditions that pharmaceutical products might encounter during storage, transportation, and distribution. It serves pharmaceutical manufacturers, research institutions, and regulatory bodies. The primary goal is to conduct stability tests on drugs, vaccines, and other pharmaceutical formulations. By subjecting these products to controlled environmental stresses, it becomes possible to predict their shelf life, evaluate potential degradation, and ensure compliance with strict industry regulations and international standards. The energy-saving aspect not only reduces operational costs but also aligns with sustainable manufacturing practices.

2. Product Features

 
  • Efficient Insulation and Durable Construction
    • The chamber is constructed with high-quality insulation materials that minimize heat transfer and maintain a stable internal environment. The walls, ceiling, and floor are insulated to prevent temperature fluctuations and maintain precise temperature and humidity levels. The outer shell is made of durable stainless steel or corrosion-resistant alloys, ensuring long-term reliability and protection against external elements. The door is designed with a heavy-duty sealing mechanism and a viewing window, allowing for easy monitoring of the test samples without compromising the internal conditions. The overall structure is engineered to withstand the rigors of continuous operation and provide a safe and accurate testing environment.
  • Precision Temperature and Humidity Control System
    • At the heart of the chamber lies a state-of-the-art temperature and humidity control system. It can achieve a wide temperature range, typically from -20°C to +60°C, with an accuracy of ±0.2°C. The humidity control range extends from 5% to 95% relative humidity, with an accuracy of ±1.5% RH. The system utilizes energy-efficient refrigeration units, heaters, humidifiers, and dehumidifiers, all coordinated by a sophisticated PID controller. Multiple sensors are strategically placed throughout the chamber to provide real-time feedback, enabling the control system to make rapid and precise adjustments to maintain the desired environmental conditions. The control system also features energy-saving modes, such as adaptive temperature and humidity setpoints, which optimize energy consumption based on the actual testing requirements.
  • Intuitive Control Panel and Data Acquisition Interface
    • The equipment is equipped with an intuitive control panel that simplifies the operation and parameter setting. Operators can easily adjust the temperature, humidity, test duration, and other parameters using a user-friendly interface. The control panel also provides real-time displays of the current environmental conditions, as well as any alarms or warnings. The chamber is integrated with a comprehensive data acquisition system. It records all relevant test data, including temperature and humidity histories, rate of change of environmental parameters, and any observable changes in the test samples. The data can be stored in a built-in memory or exported to external storage devices for further analysis. The system can also generate detailed test reports in various formats, facilitating easy documentation and sharing of results.
  • Safety Features and Alarms
    • To ensure the safety of operators and the integrity of the testing process, the chamber is equipped with a range of safety features. These include over-temperature and over-current protection, emergency stop buttons, and alarms for abnormal temperature fluctuations, humidity levels, or equipment malfunctions. The safety features are designed to prevent damage to the chamber, the test samples, and the surrounding environment, providing peace of mind during the testing operation.

3. Specific Parameters

 
  • Temperature Range and Accuracy
    • With a temperature range of -20°C to +60°C and an accuracy of ±0.2°C, the chamber can subject pharmaceutical products to a wide spectrum of temperatures. This is crucial for testing drugs that may be stored in cold chain conditions or exposed to higher temperatures during transportation or handling. The accurate temperature control ensures that the test conditions are precisely maintained, providing reliable and repeatable results.
  • Humidity Range and Accuracy
    • The humidity range of 5% to 95% RH, with an accuracy of ±1.5% RH, allows for a comprehensive evaluation of the effect of moisture on pharmaceutical products. The ability to precisely control the humidity level is essential for understanding how drugs and their packaging respond to different moisture environments, such as the hygroscopic nature of certain medications or the potential for condensation in cold storage.
  • Testing Volume and Payload Capacity
    • The chamber offers a customizable testing volume, typically ranging from 50L to 500L, depending on the specific model. The payload capacity can handle a significant amount of test samples, with a maximum capacity of up to 200 kg, depending on the size and density of the objects. This allows for efficient testing of a batch of pharmaceutical products or a single, relatively large item.
  • Data Sampling Frequency and Resolution
    • The data acquisition system samples data at a frequency of up to 200 Hz, providing a highly detailed record of the temperature and humidity changes. The resolution of the temperature data is 0.05°C, and the humidity data is 0.05% RH. This high-resolution data is invaluable for identifying even the slightest trends and potential failure points, allowing for a more accurate assessment of product performance.

4. Product Functions

 
  • Accurate Simulation of Environmental Conditions
    • The primary function of the chamber is to provide a precise and reliable simulation of temperature and humidity conditions. By subjecting pharmaceutical products to controlled environmental stresses, it allows manufacturers and researchers to evaluate their performance and durability. This is crucial for ensuring the quality and safety of drugs and vaccines, as any degradation or damage during storage or transportation could have serious consequences for patient health.
  • Product Design Optimization and Quality Control
    • Through a series of tests on different pharmaceutical product prototypes, the data obtained from the chamber can be used to optimize product designs and packaging. Engineers can analyze the behavior of various materials and components under different temperature and humidity stresses and make modifications to enhance the overall performance and integrity. The chamber also serves as a vital tool for quality control, ensuring that each batch of products meets the required environmental resistance standards. For example, in the manufacturing of vaccines, testing in the chamber can help ensure the stability of the vaccine under different storage and transportation conditions.
  • Research and Development Support
    • In the field of pharmaceutical research and development, the Energy-saving Stability Testing Chamber offers valuable insights. Researchers can use it to study the fundamental properties of drugs and their interactions with different environmental factors. They can explore new formulations and packaging materials that are more resistant to temperature and humidity extremes. For instance, materials scientists can test the performance of novel drug coatings or container materials under various environmental conditions, using the chamber to evaluate their effectiveness and paving the way for advancements in pharmaceutical technology.
  • Compliance Testing and Certification
    • The equipment is essential for conducting compliance testing to meet industry regulations and international standards. The pharmaceutical industry has strict requirements regarding the stability and integrity of products under different environmental conditions, and the chamber can be used to perform tests according to relevant standards such as ICH guidelines. The test results can then be used to obtain product certifications and ensure market acceptance.

5. Production and Quality Assurance

 
  • Stringent Manufacturing Process
    Product Tags: Pharmaceutical Stability Testing Chamber   Cold Storage Stability Testing Chamber   ODM Stability Testing Chamber  
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