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What are the benefits of package shipment testing?

What are the benefits of package shipment testing?

2022-10-21

With the rapid development of my country's e-commerce, the logistics industry is also showing a steady upward trend, and now according to the index released by the China Federation of Logistics and Purchasing, the average value is 110.3 points. Here, I will tell you the benefits of packaging and transportation parts testing. What are there? Packaging and transportation test Now its main project is to evaluate the impact of various operating steps or environmental stress on the product in the process of storage, transportation, loading and unloading, handling and distribution after the transportation packaging is designed. In simple terms, it mainly refers to the measurement and testing of the transport packaging to make the product packaging meet reasonable requirements. Through the measurement of relevant quantities in the laboratory and the targeted simulation test of the transportation package, the characteristics, structure, packaging method and materials of the product itself are continuously improved until the product packaging is as scientific and reasonable as possible with low cost. The technical performance of packaging is mainly evaluated through packaging measurement and packaging testing. This is an important means to promote packaging management, improve packaging quality, reduce losses in the process of commodity circulation, and test packaging and transportation parts to achieve packaging rationalization. It is also an effective means of arbitrating packaging accidents. Therefore, it is recommended that you correctly determine the test intensity and select the test time to make the test results closer to reality, help companies better choose packaging materials and packaging structures, control transportation and packaging costs, and predict

Sterile Barrier System Testing: The Role and Characteristics of Packaged Shipment Testing

Sterile Barrier System Testing: The Role and Characteristics of Packaged Shipment Testing

2022-11-01

Sterile barrier system test: Packaging and transport parts testing manufacturers believe that current research on e-commerce logistics packaging is basically about e-commerce packaging materials and structural design, e-commerce packaging standardization, packaging recycling, etc. Few people have studied the transportation safety testing of e-commerce logistics packaging. Therefore, it is necessary to provide research ideas for the safety test of packaging and transportation of e-commerce logistics in my country through the comparative analysis of foreign e-commerce packaging safety tests, and it is necessary to judge the hazards in e-commerce logistics. Sterile barrier system test: Packaging and transportation test manufacturers believe that most e-commerce products need to be shipped by express companies. Generally, a single piece of goods is packaged and handed over to the express company for transportation, while traditional logistics mostly use third-party logistics, so e-commerce packaging is different from Traditional logistics packaging for bulk cargo transportation in the traditional sense. Sterile barrier system test: Packaging and transportation parts testing manufacturers believe that traditional logistics packaging is mainly for bulk goods, and the customer base is relatively fixed. Logistics has the characteristics of few varieties, large quantities, large batches, and few batches. The outer packaging materials are mainly wood and cardboard, and the containers are neatly stacked inside. The quantity of transshipment is relatively small, and most of them are mechanically operated. During storage and transportation, pallets are used as carriers, and forklifts are used to move and pick goods. Packaging with e-commerce

Sterile Barrier System Testing: Some Common Sense of Packaged Shipment Testing

Sterile Barrier System Testing: Some Common Sense of Packaged Shipment Testing

2022-11-22

Sterile barrier system test manufacturers for your popular science: With the continuous development of the economy, people's awareness of pursuing a high-efficiency, high-quality, and high-service lifestyle is becoming stronger and stronger, requiring the rapid development of commodity circulation, and the logistics industry has become a support for the national economy. important pillar. The circulation of commodities is inseparable from the packaging and transportation of commodities. The purpose of packaging and transportation testing is to improve the quality and reliability of product packaging, so as to reduce the probability of product damage caused by packaging problems during transportation. Sterile barrier system test manufacturer: It is believed that the item of packaging inspection is mainly to evaluate the impact of various operating steps or environmental stress on the product during storage, transportation, loading and unloading, handling and distribution. For example: 1. Ambient temperature and humidity, to evaluate the environmental adaptability of the product during storage and transportation; 2. Stacking and compression resistance, to evaluate the pressure impact of multi-layer packaging stacking on the product during storage or transportation; 3. Packaging vibration, Assess the environmental impact of various vehicles, aviation, and sea transportation during product transportation; 4. Package drop, and evaluate the impact of accidental drop during loading and unloading on the product. Sterile barrier system test manufacturer: It is believed that transport packaging is a common form of transport packaging in the logistics and express delivery industry. Since shipping packages usually need to be shipped from one place to

Sterile barrier system testing company: Bacterial endotoxin detection method and detection significance

Sterile barrier system testing company: Bacterial endotoxin detection method and detection significance

2022-11-30

Sterile Barrier Systems Testing Company: Bacterial endotoxins are also known as "pyrogens." It is a unique structure on the cell wall of Gram-negative bacilli. Bacteria will not release it when they are alive, and will only be released outside the cell when they die. Express a variety of toxic effects, in order to distinguish from exotoxins, called endotoxins. Bacterial endotoxin is a high-content complex composed of lipopolysaccharide (LPS), protein and phospholipids. The toxic component is mainly lipid A  (Lipid  A), and maintaining A is an indispensable part of LPS activity, which can be regarded as The "biologically active center" of LPS. Located in the outer layer of the cell wall, the cell wall is covered with viscous. The endotoxins of various bacteria are weakly toxic and roughly the same, which can cause fever, microcirculation disturbance, endotoxin shock, disseminated intravascular coagulation, etc. Endotoxin is heat-resistant, stable, and has weak antigenicity. The body can produce antibodies, but there is no neutralizing effect, and anti-toxins can be formed. After formaldehyde treatment, they cannot become toxic. 1. Sterile barrier system testing company: What is the detection method of bacterial endotoxin? Sterile barrier system testing company: In the 1960s, the ancient known as "marine living fossil" was discovered

Some knowledge points of sterile barrier system testing

Some knowledge points of sterile barrier system testing

2022-12-12

Sterile barrier system test manufacturers believe that the sterile barrier system has the function of blocking microorganisms from sterile medical devices under specific conditions. Typically, packaging on the inside that comes into contact with the product is used to sterilize specific pathogens for sterile medical devices. The types of sterile barrier systems include: disposable sterile barrier systems, which achieve sterile barrier function through sealed packaging; or single-use reusable packaging materials, which achieve sterile barrier function through airtight packaging; reusable sterile barrier The system can achieve sterile barrier function through valves or filter assemblies. Sterile barrier system testing manufacturers believe that since medical devices are sterilized after packaging, the packaging material and/or system should be able to withstand the sterilization process and meet the conditions required for sterilization in packaging. For sterile medical device manufacturers, the design and material selection of sterile packaging should take into account the specific characteristics, intended use, validity period, transportation and storage conditions of the medical device, and should be compatible with the sterilization process to meet the requirements of sterilization, packaging content Basic requirements for material protection and sterilization medium discharge. Sterile barrier system test manufacturers believe that the basic requirements of aseptic packaging mainly include the following aspects: (1) The integrity of the packaging. Including seal integrity and seal integrity; (2) Stability of packaging materials. keep packing material

How to perform bacterial endotoxin test

How to perform bacterial endotoxin test

2022-12-30

Bacterial endotoxin is a unique structure of Gram-negative bacilli in the outer layer of the cell wall. As an exogenous source of heat, endotoxin can neutralize cells, etc., release endogenous pyrogens, act on the thermoregulatory center, and induce heat. Bacterial endotoxin detection is the structure of the outer layer of the cell wall of Gram-negative bacilli. As an exogenous heat source, neutrophils, etc. release endogenous heat source substances, which act on the body temperature regulation center to generate heat. The main chemical component of bacterial endotoxin is lipopolysaccharide (LPS). Lipopolysaccharide contains three components: fat A, core polysaccharide and O antigen. Among them, fat A is a kind of saccharin, which is the toxic part of endotoxin and is closely related to dental disease. relevant. Existing widely in nature, it is mainly released when Gram-negative bacilli die or attach to other cells. For example, the amount of endotoxin contained in tap water is generally 1 ~ 100 EU/ml. Endotoxins can enter the body through the digestive tract without causing harm. Entering human or animal blood by injection etc. can cause other diseases or death. Therefore, it is particularly important to detect bacterial endotoxins such as medical devices, pharmaceuticals, dialysis fluids, and injection water. At present, the detection method of bacterial endotoxin is mainly based on the reagent detection method. According to the particularity of some drugs, they cannot

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