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Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Specifications
Brand Name :
PRECISION
Model Number :
TC-800
Certification :
ISO
Place of Origin :
CHINA
MOQ :
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
Temp range :
+150~-70℃
Humidity range :
10% ~ 98% R. H
Internal material :
304 Stainless Steel
External material :
Powder coated #304 Stainless Steel
Temperature Uniformity ℃ :
0.01
Humidity Uniformity % R. H. :
0.1
Temperature stability ℃ :
±0.3
Description

Custom Temperature - Humidity Environmental Chamber: The Key Force in Guarding the Quality of Drug Packaging Materials

1. Introduction

In the pharmaceutical industry, drug packaging materials play a crucial role. They not only protect drugs from external environmental influences but also ensure the quality and safety of drugs throughout their shelf - life. Different drugs have diverse requirements for packaging materials, ranging from solid tablets to liquid medications. The custom temperature - humidity environmental chamber is designed to meet this need. It can simulate various temperature and humidity conditions that drugs may encounter during storage and transportation, helping pharmaceutical companies and packaging material suppliers comprehensively evaluate the performance of packaging materials and providing a solid support for ensuring drug quality.

2. Key Features

2.1 Precise Temperature and Humidity Simulation

  • Wide - Range Temperature Control: The test chamber can achieve a temperature adjustment range from 2°C to 60°C, capable of simulating the low - temperature environment required for refrigerated drugs as well as the high - temperature environment in hot climates. At the low - temperature end, it can simulate the storage conditions of refrigerated drugs such as insulin and other biopharmaceuticals, ensuring that the packaging materials can still maintain good barrier properties and physical stability at low temperatures. At the high - temperature end, it can simulate the environment when drugs are transported or stored in high - temperature regions in summer, detecting whether the packaging materials will deform, age, or reduce their protection ability for drugs at high temperatures. The temperature control accuracy can reach ±0.5°C, ensuring the accuracy and repeatability of test conditions.
  • Accurate Humidity Regulation: The humidity adjustment range is from 20%RH to 95%RH, with an accuracy control of ±3%RH. High - humidity environments may cause drugs to become damp and moldy, while low - humidity environments may cause certain drugs (such as soft capsules) to crack or lose moisture. By precisely simulating different humidity conditions, the moisture - barrier performance of packaging materials can be tested, as well as their stability during humidity changes. For example, for moisture - sensitive drugs, the ability of the packaging materials to effectively prevent moisture ingress can be tested in a high - humidity environment, thus ensuring that the quality of the drugs is not affected.

2.2 Flexible Customized Design

  • Size and Layout Customization: According to the different sizes and shapes of drug packaging materials, the internal size and layout of the test chamber can be customized. Whether it is a small medicine bottle, medicine box, or large - scale infusion bag packaging materials, they can be properly placed and tested in the test chamber. The internal space can be partitioned according to customer needs to simultaneously test multiple different types of packaging materials, improving the test efficiency.
  • Customization of Sample Fixation and Testing Methods: To ensure that the packaging materials can accurately simulate the actual use state during the test process, specialized sample fixation devices and testing methods can be customized. For example, for film - type packaging materials, special fixtures can be designed to subject them to temperature and humidity tests in a stretched state, in order to evaluate their performance changes during the actual packaging process; for bottled drug packaging, the stacked placement method can be simulated to test the temperature - humidity barrier performance of the packaging materials when under a certain pressure.

2.3 Advanced Monitoring and Control Systems

  • Intelligent Control System: Adopting an advanced intelligent control system, users can easily set various test parameters, such as temperature - humidity change curves, test time, and cycle times, through the human - machine interface. The system also has functions of fault diagnosis and alarm. Once abnormal situations such as temperature - humidity runaway and equipment failure are detected, it can immediately issue an alarm and take corresponding protective measures to ensure the safety and reliability of the test process.

3. Technical Parameters

Parameter Items Details
Temperature Range 2°C to 60°C
Temperature Accuracy ±0.5°C
Humidity Range 20%RH to 95%RH
Humidity Accuracy ±3%RH
Internal Dimensions Customized range: Length Min 400mm to 3000mm, Width 400 mm to 3000 mm, Height 500 mm to 3000mm
Data Collection Frequency Adjustable between 10 times/second and 10000 times/second
Power Requirements 380V, 50/60Hz,

4. Benefits for the Drug Packaging Material Industry

4.1 Improve the Quality and Reliability of Packaging Materials

  • Comprehensive Performance Evaluation: By simulating various temperature and humidity conditions, the performance of drug packaging materials can be comprehensively evaluated, and potential quality problems can be discovered in advance. For example, testing the sealing performance of packaging materials in high - temperature and high - humidity environments can effectively prevent drugs from being contaminated or deteriorated due to poor packaging sealing during actual storage and transportation.
  • Optimize the Selection of Packaging Materials: Based on the test data provided by the test chamber, pharmaceutical companies and packaging material suppliers can more scientifically select packaging materials suitable for different drugs. For example, for humidity - sensitive drugs, packaging materials with high barrier properties can be selected, and their effectiveness under different humidity conditions can be verified through tests, thereby improving the stability and shelf - life of drugs.

4.2 Reduce Costs and Risks

  • Reduce Drug Loss: Well - tested packaging materials can better protect drugs and reduce drug loss caused by poor - performing packaging materials. This not only reduces the production costs of pharmaceutical companies but also reduces the risks of recall and compensation due to drug quality problems, maintaining the brand image of enterprises.
  • Shorten the R & D Cycle: The test chamber can quickly simulate various temperature and humidity environments, accelerating the R & D and testing process of packaging materials. Compared with traditional field - testing methods, it greatly shortens the R & D cycle, enabling enterprises to bring new products to the market faster and improving their market competitiveness.

4.3 Meet Regulatory and Market Requirements

  • Ensure Compliance: The pharmaceutical industry is strictly regulated, and there are clear requirements for the performance and safety of drug packaging materials. The custom temperature - humidity environmental chamber can help enterprises conduct tests that comply with regulatory standards, ensuring that the packaging materials meet relevant regulatory requirements and can pass the review of regulatory authorities smoothly.
  • Enhance Market Adaptability: With the increasing attention of consumers to the quality and safety of drugs, the requirements for drug packaging materials are also becoming more and more stringent. By using the test chamber for comprehensive testing, enterprises can produce packaging materials that better meet market demands and enhance the market competitiveness of their products.

5. Application Scenarios

5.1 Packaging Material R & D Stage

  • New Material Performance Testing: When developing new drug packaging materials, the test chamber can be used to test the physical properties (such as tensile strength, flexibility, air permeability, etc.) and chemical properties (such as antioxidant properties, corrosion resistance, etc.) of the materials under different temperature and humidity conditions, and evaluate whether they are suitable as drug packaging materials.
  • Formula Optimization: For existing packaging materials, by simulating different temperature and humidity environments in the test chamber, the influence of different formulas on the performance of the packaging materials can be tested, so as to optimize the formula and improve the performance and stability of the packaging materials.

5.2 Packaging Material Quality Control Stage

  • Batch Sampling Inspection: During the production process of packaging materials, sampling inspection is carried out for each batch of products. The test chamber is used to simulate the storage and transportation environment of drugs, and the performance indicators of the packaging materials are detected to ensure that the quality of each batch of packaging materials is stable and reliable.
  • Supplier Evaluation: When pharmaceutical companies select packaging material suppliers, they can require suppliers to provide performance reports of packaging materials tested in the test chamber, or conduct independent tests on the samples provided by suppliers, so as to evaluate the product quality and stability of suppliers and select high - quality suppliers for cooperation.

5.3 Drug Stability Research Stage

  • Packaging - Drug Compatibility Testing: Put the drugs and packaging materials together in the test chamber, simulate the actual storage conditions, observe the interaction between the drugs and the packaging materials under different temperature and humidity environments, and evaluate whether the packaging materials will affect the quality and stability of the drugs, ensuring good compatibility between the drugs and the packaging materials.
  • Accelerated Stability Testing: By setting higher temperature and humidity conditions in the test chamber, accelerated stability testing of drugs is carried out to predict the shelf - life of drugs under normal storage conditions and provide a scientific basis for setting the expiration date of drugs.

Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging MaterialsCustom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials

6. Conclusion

The custom temperature - humidity environmental chamber, as a key device for ensuring the quality of drug packaging materials, provides a comprehensive and efficient testing solution for pharmaceutical companies and packaging material suppliers with its precise temperature and humidity simulation ability, flexible customized design, and advanced monitoring and control systems. It not only helps to improve the quality and reliability of packaging materials, reduce costs and risks, but also meets the strict requirements of regulations and the market. If your enterprise needs such a reliable test equipment in the R & D, production, or quality control process of drug packaging materials, please feel free to contact us at any time to learn more about the custom temperature - humidity environmental chamber. Let's work together to contribute to the quality improvement of drug packaging materials.
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Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials

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Product Detail
Brand Name :
PRECISION
Model Number :
TC-800
Certification :
ISO
Place of Origin :
CHINA
MOQ :
1
Price :
$6000
Contact Supplier
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Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials
Custom Temperature Humidity Environmental Chamber Key Force In Guarding Quality Of Drug Packaging Materials

Dongguan Precision Test Equipment Co., Ltd.

Verified Supplier
1 Years
guangzhou
Since 2006
Business Type :
Manufacturer, Exporter, Trading Company, Seller
Main Products :
Environmental Test Chambers, Climatic Test Chamber, Thermal Shock Test Chamber
Total Annual :
5000000-10000000
Employee Number :
50~100
Certification Level :
Verified Supplier
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