In May, in addition to the formal implementation of the zero-tariff policy for anti-cancer drugs, there is also a new regulation that will affect pharmaceutical companies, that is, "Technical Specifications for Confirmation of Performance Verification of Equipment for Cold Chain Logistics of Temperature Control Facilities for Pharmaceutical Products" (hereinafter referred to as "Code") ). On the 3rd, the "Regulations" press conference was held in Beijing. At the press conference, experts and scholars specifically introduced the drafting of the "Code" and the importance and significance of its implementation. According to relevant news reports, the "Specifications" was officially implemented on the 1st.
What kind of content has the "Specifications" specifically formulated? For the current pharmaceutical circulation industry, what role will the "Regulations" play? What impact will it bring to pharmaceutical companies? How should companies follow to follow? The author collected relevant information for analysis.
The "Code" will improve the operation level of the drug cold chain to ensure the safety of the people's medication
The author understands that the "Specifications" was proposed and managed by the National Logistics Standardization Technical Committee and was drafted by 14 units. It mainly stipulates the content, requirements and operational points of the verification performance verification of temperature control warehouse, temperature control vehicle, refrigerator, incubator and temperature monitoring system involved in cold chain logistics of pharmaceutical products.
At the press conference, relevant experts gave a detailed introduction to the formulation and implementation of the Code. Among them, Qin Yuming, executive deputy head of the Pharmaceutical Logistics Standardization Working Group of the National Logistics Standardization Technical Committee and Executive Vice President of the China Federation of Pharmaceutical Logistics, said that he hopes to improve the coverage of the Code of Practice for Pharmaceutical Cold Chain Logistics through the Code. The level of operation of the drug cold chain. Yu Rui, general manager of Beijing Keyuan Xinhai Pharmaceutical Management Co., Ltd. hopes to form a standard unified verification market through the implementation of the "Specifications", improve the quality management level of enterprises, and ensure the safety of the people's medication.
Competition in the pharmaceutical circulation market will intensify cold chain equipment companies will face greater challenges
In fact, for the pharmaceutical circulation industry, the competition is huge, not only the enterprises that are mainly based on this, but also the third-party logistics enterprises. Many companies have entered the pharmaceutical circulation market, which undoubtedly saw its huge commercial value and market potential. According to relevant data, in 2017, China's pharmaceutical logistics totaled 3.02 trillion yuan, a year-on-year increase of 11.3%. According to the annual growth rate of 8%, by 2020, China's total medical logistics is expected to reach 3.8 trillion yuan. In addition, there are also data showing that the market size of China's cold chain transportation drugs will reach 80 billion yuan.
The considerable market prospects have attracted many pharmaceutical companies to join, and the market competition has become more intense, and the implementation of the "Code" will continue to accelerate the intensity of this competition. Because the "Specifications" have clearly defined the requirements for equipment required for cold chain logistics of pharmaceutical products, equipment or enterprises that do not meet the standards will be eliminated. Therefore, many enterprises are seeking and updating a batch of cold chain equipment. It can be seen that cold chain equipment companies will face even greater challenges in the future.
The specific "Specifications" are coming! How should cold chain equipment companies respond?
In the pharmaceutical cold chain logistics market, familiar people are aware of the "vaccine" incident that has been heated up. This is a vaccine market with huge market opportunities. Due to the shadow of this incident, many pharmaceutical companies have been affected, and the incident has also sounded the alarm for the pharmaceutical cold chain logistics industry. As a result, the state has attached great importance to the pharmaceutical circulation industry, strengthened supervision and cracked down on illegal activities. The implementation of the "Code" will further bring strict normative role to the industry and related enterprises to ensure the quality and safety of drugs.
So, how should pharmaceutical companies, especially cold chain equipment companies, meet the challenges? First of all, cold chain equipment companies should strictly follow the "Specifications" to eliminate products that do not meet the requirements. Secondly, enterprises need to produce equipment according to the standard, meet new requirements, and escort the quality and safety of drugs. Finally, cold chain equipment companies should also actively research and develop, and promote the healthy development of the industry through innovation based on the "norms". Other pharmaceutical companies also need to comply with the requirements of the "Specifications" to ensure the quality and safety of drugs from the aspects of equipment, transportation and medicine. Only in this way can the pharmaceutical cold chain industry be more standardized and developed, and the safety of people's medications can be more protective.
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