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Things security traffic is expected to become the fastest growing areas of medical
Chinese community in Wuxi at the second China Internet of Things (sensor network) Fair published "2010-2011 annual report of China Internet of Things" (the "Annual Report") expected over the next five years, the global networking industry market will show rapid growth in 2012 or more than $ 170 billion in 2015 to nearly $ 350 billion, an average annual growth rate of nearly 25%. This is the second consecutive year, Xinhua News Agency released the special annual report.
Report said, with safe urban construction, urban intelligent transportation system and the "new medical reform" to speed up the construction of medical information, security, transportation, and the three major areas of health care is expected to take the lead in the development of things to benefit the networking industry to become the largest market capacity , the most significant growth areas.
Report studies suggest that perceived level of networking technology, including technology, technology and application layer network layer three levels of technology. Among them, the perception layer technology, the most important things is the basis of the sensor, sensor technology and short-range wireless communications technology is the current technology research things hot and difficult.
Currently, the domestic low-frequency and high frequency RFID technology has matured, but the UHF and microwave bands are still lagging behind with foreign; sensor technology and a big gap between U.S. and European countries such as Japan and South Korea. The network layer technology after ten years of rapid development, has a more mature and can basically meet the current demand for networking applications.
From the time dimension, RFID and sensor vendors will use in the networking industry s first to benefit from the process, followed by system integrators, operators of things. From the space dimension, the biggest room for growth is the operator of things, followed by system integrators, and then after RFID and sensor suppliers.
Annual report of that at present, China s development of things is still faced with many deep-seated contradictions and problems. Industry on the whole, things are still in the conceptual import and the formation of the initial stage of the industrial chain, the networking industry s core technologies are not exceeded, the manufacturing process level is not high, chain link poor, low-level applications, business model is not enough clarity, lack of resource sharing. Of particular note is the construction of things over there in the duplication of investment and disorderly development. Development stage of China s Internet of Things should be transferred as soon as possible to the product, industry, demonstration, commercial, market-core stage of development.
EIZO released for medical imaging diagnosis of 8-megapixel color display
China, October 18, 2011 – Eizo announced that it would release a new medical imaging can be applied to all aspects of the 8-megapixel ultra-high-resolution color display diagnostic RadiForceRX840.
In the medical field, the use of non-film mode imaging applications speedily and hospitals need to address the growing image type and amount of information. RadiForceRX840 has a 36.4 inch screen size, display the information amounted to 8 megapixels (4096×2160 native resolution), but with no unsightly border. The display has a wide space that can display all the necessary imaging applications or windows.
EIZO RX840 is the first use of LED (light emitting diode) backlight medical displays, and traditional CCFL (cold cathode fluorescent lamp) backlight different, LED backlight will decay much slower, thus extending the life of the monitor. Quality assurance of products specifically illustrated, the display in 5 years or 25,000 hours can be maintained in the recommended values ??of up to 400cd/m2 brightness. This guarantee ensures that the required diagnostic monitor stable and reliable performance.
RX840 with EIZO\\ s proprietary hybrid gamma function, which even in the same application can also automatically distinguish between the displayed image is monochrome or color. Display monochrome images, the display will be adjusted using the standard model by DICOMPart14; and display color images, then use the model by adjusting the gamma 2.2. This feature color and monochrome by ensuring that medical images can be displayed simultaneously to the best way to expand the PACS (picture archiving and communication system) availability.
Tilt angle of view from three screens, RadiForceRX840 display panel used in almost no detectable color. 176-degree wide viewing angle range, can watch over the same time.
RadiForceRX840 installed in front of the border at an IFS (integrated front sensor), the user can develop a plan to measure gray tones, but also the school transferred to DICOMPart14 standards. Install the supplied RadiCSLE software, IFS and RadiCSSelfQC feature allows monitor their implementation of quality control tasks, even if the connected workstations can also be closed. This feature greatly reduces the workload monitor quality control and maintenance costs.
52 private medical institutions advertising “deviant” fined
As the press release medical advertisements are strictly limited, part of the medical institution to use the Internet from print publications or publishing illegal medical advertisements, the same harm to the patient and his family can not be underestimated. Yesterday, the Shanghai Municipal Health Bureau, Health Authority announced to the public in the third quarter of the city investigation of illegal medical advertisements, the city a total of 52 private medical institutions as punishable by law.
Shanghai Yangtze River Hospital, Shanghai Medical Beauty big hospital, Shanghai anal Thai Hospital, Shanghai Peoples Hospital, Shanghai New Hongqiao Hospital, Shanghai Concert Hospital, Hai on the city such as the eye clinic 52 private medical institutions, as the Internet, self-printed publish illegal medical advertisements, or tampering with the contents of the audited medical advertising, health administrative departments shall be investigated.
Things: the medical industry opportunities and challenges
Things will affect residents in all aspects of medical and health behavior, medical institutions to provide behavior, and the future of health policy, it also requires management to promote innovation and change.
First, a new round of medical reform plan things in advance is no doubt the field of health care an important opportunity for development. The success of the new medical reform, an important evaluation is whether the residents to address \"difficult and expensive\" problem. In addressing the \"difficult\", the application of things that people can use a PC, terminal services, community information, and even cell phone networks to achieve personal account login, register for an appointment anytime, anywhere, online consultation, check their health status and access personalized preventive and rehabilitative guidance; in the hospital, registered, designated price, fees and reimbursement will be directly through the network, greatly simplifying the process for medical treatment to alleviate the queuing problem. In addressing the \"expensive\" side of things so that pharmaceutical production – distribution – sales of the link displayed in public, not only for drug addition, an effective monitoring, drug safety also play a role in safeguarding. Seeking behavior of a fee for each real-time review by the health insurance department links automatically reimbursed for the documents do not meet the principle of reimbursement will be timely feedback to the physician-patient service terminal, and similar scenarios generated by the database processing program other doctors for reference. Conducive to health insurance supervision department of the hospital, and it helps statistics commonly used in the clinical use of drugs, dynamically updated essential drug list.
Second, things to bring the integration of resources and information sharing, and ultimately will lead to information disclosure, administrative transparency, make public a government decision-making, health care system an important part of running. The current field of medical information does not form a whole, the data is less than open, such as hospitals, performance evaluation, the result is only relevant administrative departments within the hospital and hold in the general population is difficult to obtain relevant data. The emergence of things people will provide as a service system into the core system, play the role of public scrutiny, which will help the hospital compete with each other to learn and improve service delivery level. In addition, things in the field of universal health care, the industry will change the traditional pattern. As mentioned above, the development of things required medicines, medical supplies, equipment, and so all access to network-related products, from raw materials into finished products used in the factory to the patient, the whole process will be left on the network can be queried record. This also means that the process of production and distribution of related products will be an open, transparent, fully exposed to public scrutiny.
Third, the Internet of Things should encourage private participation, promote healthy competition. However, IC card, RFID tags, HIS system once applied in the field of health care, they will be with the nature of some public services. Medical field in particular, is experiencing a \"sooner, center of gravity\" of the reform, the future focus is to improve health services accessibility, fairness. Therefore, the Government must be the appropriate guidance. Health resources to avoid the big cities, over-concentration of large hospitals, to bring residents to prevent the digital divide between rich and poor differentiation intensified. Internet of Things technology and community health services, medical insurance combined, so that residents can truly enjoy the convenience of things.
Things in convenience, but also brought some new problems, whether related industries and medical fields complement each other, to achieve information disclosure, management is able to break the bars separated, sharing resources, is a major management challenges. In addition, a unified coding standard, the industry regulatory rules, privacy protection, and also the PPP co-operation of China\\ s development of things should be solved the problem. From the recent process of health information technology can be seen, things will be the promotion of health care and related fields in the set off a new revolution. Synchronization with the new technology from the concept of management changes and challenges, how to seize opportunities in the global trends in difficulties, is the top priority of the next government. I believe in the institutional transformation in the future, things will play a major role in opening the field of health care situation.
Medical integrators five new skills
With the \"new medical reform\" of the unfolding, the Ministry of Health carried out jointly by the seven departments of the \"safe hospitals\" to create activities progress, and in the \"1025\" period of building a core of electronic medical records for the application of information technology file system and the health of residents of the regional service platform as the core of medical information technology reform, combined with high-definition network security industry, the application of IP technology continues to mature, most hospitals into high-speed network, the establishment of a significant data processing capacity of hospital information systems, regional health care information systems and electronic medical records market under the guidance of national policy the rapid development of large-scale data center construction and integration between application systems show a trend.
The medical profession not only integrator needs to guide the direction of the new hospital, is going to follow this new trend of technological change, upgrade existing technology, and continue to learn and master new skills, make new era of health care industry, security integrators.
Digital trend, to be cross-sectoral collaboration
In recent years, with the physician-patient relationship of tension and other reasons, the hospital system of concern about the increasing security, security systems and the application of digital hospital is also showing a combination of new features. Installation with previous hospital management of each building a separate analog control systems, digital hospital to the application of computer, communications, multimedia, networking and other information technology, disease prevention, care, treatment, care, automation of business management and administration digital operation, to achieve the hospital\\ s medical treatment, teaching, research and management to achieve network. To accomplish such a vast and complex engineering, medical industry, integrators need to communicate with the relevant departments for multi-collaboration efforts to meet the security needs of the different characteristics of departments to build the best fit their application needs security system.
To different functional areas within the hospital\\ s security system for different needs, for example, patient registration hall traffic flow, access to personnel as complex, requiring high-definition monitoring equipment; storeroom and storage of valuable equipment, library and other valuable things on fire has strict security requirements. British product manager Shu-Fen Wang talked about this, said: \"The medical industry integrators in the construction process with the different departments to maintain adequate communication, understanding the different departments of the hospital business processes and its system architecture needs; addition , the integrator needs to focus performance security products and positioning, demand for the different hospital departments to provide the most appropriate security products, to hospitals in different functional areas to meet different security requirements, but also to all security subsystems are integrated in the digital Hospital under the management of a large platform. \"
Since the investment in gold, continuous integration build test
Most general hospitals are usually part of the construction funds from local financial approval, part of the funding comes from the self and society. British Shu-Fen Wang said that \"although the hospital building, diversification of funding sources, but the investment in hospitals in all parts of the distribution ratio determined by the hospitals themselves. Now, for the hospital\\ s investment in the weak system relatively small proportion, the majority of hospital generally choose to build the basis of information in part with funds after the late addition there is a need for the security system, security system in stages to the hospital the digital upgrade. \"benefits of doing so is to ease the hospital\\ s capital pressure, but the hospital information construction stages stretched too thin, the whole hospital is not conducive to the integration of security systems, likely to cause conflicts or different system architecture security is not compatible between brands, will for the post-maintenance as well as a huge digital upgrade difficulties and obstacles.
To solve this problem it is necessary to have the ability to integrate the different subsystems and between different security compatibility between brand-name products. Necessary to be able to integrate different periods and different technical standards of security systems, such as time to be able to use analog integrated analog and digital security systems in the process of upgrading the new IP network system, or is capable of SD and HD monitoring for unified management, but also to the different functional areas of the different building integrated unified security management subsystem, such as the hospital all the video surveillance, access control, fire, police are unified into a management platform for intelligent interaction management, not only from security point of view play a more effective role, from the management level is also an effective way to improve management efficiency.
Demonstrate new technologies to improve market awareness
Currently in the hospital, in addition to traditional security applications, the number of new applications are increasingly prominent, the future of the medical industry needs new technology and equipment, such as, Internet of Things technology, high-capacity storage, information technology solutions for the whole hospital, the department image fusion, intelligent video analysis, high-definition imaging solutions, card systems, RFID applications, the unified platform management subsystem. Beijing Xin Zhuo more technology development limited liability company president Tu Jing said: \"For hospitals, the user is not familiar with some of the emerging technologies and equipment, the need for engineering companies demonstrate and explain the corresponding Party, meanwhile, lead the user to visit a successful model case, allowing users to learn about new technologies and new equipment in practical applications is how to play a role, how to make hospital management more convenient, improve customer for new technologies, equipment, awareness, so that emerging technologies can successfully enter the market . \"
The successful promotion of new technologies and new equipment, integrators must be within the hospital and construction features in-depth understanding of the process, especially for operating rooms and special areas of construction capacity. The network monitoring system, installation of equipment and more demanding, such as surgical teaching system, related to the multimedia industry expertise, it must be experienced in many fields of engineering business to complete.
Meanwhile, for the hospital\\ s own special needs and upgrade their digital stages of the construction characteristics of the process, contractors must take into account the complete system solution is also very important, which requires equipment manufacturers and engineering companies very detailed understanding of the the demand for hospital characteristics. Beijing Xin Zhuo more Tu Jing said: \"Contractors have to enter the medical field, we need to have strong design and construction capabilities, intelligent system integration capability, high-level intelligent system integration qualification, qualification and other computer systems integration, integration business itself, but also to learn new techniques, constantly on their reserve team updates on the technical knowledge to collect market demand dynamics, together with the relevant manufacturers to meet the industry needs to discuss the characteristics of new products and to market. \"
Control features to meet the different needs of the industry
In general, large general hospitals, such as the top three hospitals qualified for the integrators have very strict requirements, such as Security Project qualification, building intelligent contractor qualifications, computer system integration qualification, some security-related construction software development needs double soft certification , national high-tech enterprises, did not meet the relevant qualifications to undertake the project integrator is not the.
Large general hospital area is very large, and base building and more building functions clearly differentiated, internal medicine and surgery, gynecology and pediatrics, the presentation of the features are not the same, the required security systems are not the same. Integrators need to install different functional areas of the different characteristics of the security features of the system to meet the needs of their differentiation. Import and export of hospital, inpatient corridor, operating room, placed at the expensive medical equipment, drug supply, mobile workers gathered at the (lobby, elevator, cashier, at the dispensary) and focus on the design of hospital security. Hospital building and medical equipment placed at the expensive, drug supply not only the main fire alarm, alarm system also needs the help. Hospital departments focus their security resources from public places, sent to the Security Section; and some emergency needs of the emergency command transmitted to the Presidency for the first time on-site management; In addition, for multimedia conferences, teaching The recording / playback, and more classes for university affiliated hospital; the care of critically ill patients, visits, etc. are managed mainly by the medical staff.
Operating characteristics from the hospital point of view, different hospital systems focus on the required security is not the same, different types of hospitals such as mental focus to quickly locate information, patients can quickly check which location and duration of stay; door for a long time did not turn off alarm, that the door is open or forget to close a long time, the system control interface software will prompt the red alarm time and location, and drive the computer speakers to remind duty attention. The nature of the medical research focuses on the use of laboratory safety, drug safety management, as well as to avoid animal experiments emergencies. Often these places will be divided into different risk levels, according to different risk levels integrators security needs as well as from the customer\\ s individual needs, the formation of different security solutions.
Establish industry standards to promote the process of digital hospital
With the hospital\\ s concern for the security system is increasing, the hospital has the appropriate functions within the management, maintenance and operation security system. Beijing Xin Zhuo more Tu Jing said: \"In recent years, a number of engineering and manufacturers also felt the hospital awareness of security systems, has greatly exceeded the traditional thinking inherent in the current system, many hospitals have realized the importance of security and said strong demand for security. \"
On the status of the medical profession is concerned, there is no industry standard for a specific medical mandatory normative documents, which makes many medical institutions in the digitization process of upgrading the lack of a benchmark.
For this, the British of Shu-Fen Wang said: \"As the number of China\\ s medical industry, the lack of standards, so many are willing to try the latest technology, a large hospital turned to international standards JCI, JCI is a universally accepted standard of medical service standards , on behalf of the hospital services and hospital management, the highest level. \"JCI standard covers 368 standards (including the core standards 200, 168 non-core standards), but also contains several of each standard measure under the elements. \"One of public facilities and safety management, quality improvement, hospital leadership, coordination and cooperation, and information management-related standards in the digital upgrade of the hospital in an important basis for the transformation process.\" She said.
In addition, high domestic labor costs is not the number of China\\ s medical industry is one of the obstacles in the process. Shu-Fen Wang said: \"Many hospitals do not realize that the digital upgrade of the true meaning, preferring to hire more labor to replace anti-technology management in the role of hospital security.\"
But to achieve real security, for the safety of hospital patients to provide quality service, must be implemented air defense, anti-technology, anti-material combination, can effectively prevent loss, mitigate risks, improve the safety factor. Medical industry integrators have to actively participate in the discussion to the industry standard for the future of China\\ s medical industry provide the basis for the establishment of standards.
New model of medicine has brought new opportunities for medical device regulation
Aerospace technology, new materials, digital information technology and other new technologies, the rapid development and the different technologies between the increasingly integrated in the promotion of medical device industry developed rapidly, to meet public health needs, the medical device industry and regulators have formed a new opportunities and new challenges.
China Academy of Engineering, Yu Meng-sun, vice chairman of China Association of medical equipment and other insiders have pointed out that Dai Jianping, a gradual shift from the medical model is disease-centered to changes in the health center, rapid economic development, new medical reform to increase investment and residents increasing emphasis on health, both medical device industry will bring tremendous opportunities and broad space for development. Changes in the industry and at the same time, medical supervision should be adjusted accordingly ideas.
Regulatory and industrial development are mutually reinforcing aspects. State Food and Drug Administration (SFDA) A deputy director-side vibration that the medical equipment industry\\ s rapid development, to the supervision brought many new opportunities and challenges. With the protection of armed security people on the basis of this fundamental, regulatory authorities will provide the policy support, management and information services, and promote further standardize the market order for the industry to create a healthy sustainable environment.
New model brings new opportunities
With the sustained rapid growth, new medical reform in the government to increase investment to strengthen primary health care institution-building, people\\ s health conscious and aging population, under the influence of various factors, the medical device industry ushered in unprecedented opportunities for development. Qilu Securities analysts believe the next three years, the global medical device growth is expected at 4% to 6% in 2011, global medical device market will reach $ 312 billion, while the expansion of China\\ s market growth rate will reach 20%. Among them, the home medical equipment will show a rapid development momentum, is expected to portable home medical equipment industry in the next three years, the overall growth rate of 30% or more.
Although in recent years, China\\ s medical device industry was the rapid development, but with the international advanced level, there are still a considerable gap. Yu Meng-sun that, in accordance with disease-centered medical model, China\\ s medical device industry to reach the world advanced level is very difficult to recover the greater the gap even more. The current development of China\\ s medical device industry to a turning point, may lead to better medical direction, may also lead a bad direction. Only by changing the medical model, to play China\\ s inherent advantages, it may be changed from the catch-up leader.
In fact, medical and health industry has been aware of the disease-centered model of medical limitations. World Health Organization made it clear that the medical center should shift to the disease-health center. This medical device industry, pointed out the direction for future development. Accordance with the health center\\ s medical model, Yu Meng-sun that medical services in health status should be toward the identification and adjustment of the direction. Chinese traditional medicine culture is a holistic thinking, dialectical therapy, health-centered model, therefore, China has a unique advantage in this respect, if to seize this opportunity, combined with modern science and technology, China\\ s medical device industry has may walk in the world.
Dai Jianping Yu dream Sun strongly endorses the view, and further detailed analysis of the medical pattern to bring changes in the medical device industry: from the treatment for the symptoms, to identify and conditioning for the sub-health; mainly from invasive to non-invasive, minimally invasive direction ; shift from the past for community hospital services and family services. This analysis coincides with Qilu Securities.
Dai Jianping also pointed out that medical devices have two major trends in technology, one from the digital to the network, wireless network development, and the other is the continued integration of various technologies, such as PET-CT and later appeared in PET-MR.
To regulate and promote development
Whether the establishment of a new model of medical or health care needs of residents, driven, and new technology development and integration, these factors contribute significantly to development of the industry, but also to the regulation of medical devices has brought unprecedented challenges.
Yu Meng-sun pointed out that with the medical model changes, changes in medical device development, regulatory thinking should be adjusted accordingly, to determine the effectiveness of the product should not be disease-standard, but health status should be the standard. Dai Jianping also proposed, network technology, nuclear medicine, radiology and other fusion techniques, has brought many new problems, such as healthcare IT ethical issues, PET-MR fusion products such as nuclear medicine or radiology are , and so on. Whether it is the development of concepts, methods or techniques, gave a huge regulatory challenges,
As Dai Jianping said, development is the prerequisite for regulation, supervision is the development of protection. Mechanical security with the public, industry, health and sustainable development are inseparable from the scientific supervision. At the same time, companies have developed, standardized, it can reduce regulatory pressures and risks.
A side vibration that protect public safety with firearms is a fundamental medical device regulation. On this basis, the regulatory authorities will strive for the development of enterprises to provide more help and services, promote healthy and sustainable development.
China\\ s medical device regulatory history is not long, in recent years, regulatory capacity and level has been improved significantly. Contrast in the past, or even with the enormous changes. Medical device regulatory laws and regulations, technical support system, detection system, adverse event monitoring system have gradually established and perfected, the unification of the national registration and approval of medical devices, production and management supervision, adverse event monitoring. \"Continue to reinforce the regulatory basis of public safety with effective mechanical protection.\" Edge vibration A historical review of China\\ s medical device regulation, said.
For businesses concerned about the more ultra-approval time, grasp around the inconsistencies in the approval of the standard problems, while a vibration that, SFDA attaches great importance to the views of business, make great efforts to improve capacity and efficiency review. This year, compiled by the Office agrees, SFDA equipment review center staffing from 30 to 100; in order to improve the efficiency review, review center also conducted within the institutional reform. Through these efforts, review of equipment over time the problem has been basically solved.
Review in order to regulate behavior, uniform review of scale to help businesses research and reporting, review of regulatory authorities also actively developing technical specifications. Lu Aili, deputy director of Beijing Municipal Food and Drug Administration, said the Beijing bureau in the country since 2005 to develop and publish the first review of technical specifications, so far has publicly released the 30 specifications, covering about 50% of the species, \" where there are norms have accelerated the speed of review. \"
A side vibration that \"five-second\" period, both the medical device industry or medical device regulation, will usher in a new leap forward. SFDA supervision in the medical device further improve laws and regulations, improve standards, strengthen supervision, scientific monitoring and research into a reasonable state Bureau, Provincial Bureau, Council\\ s powers to improve the efficiency of supervision. At the same time, doing service work for the industry to create a healthy and sustainable environment. I believe the next five years, government and industry through the joint efforts of the medical device industry will usher in more development opportunities, to be developed faster.
MEMS sensors market to accelerate the development of medical electronics
Chinese medical electronics, especially portable medical electronics industry\\ s rapid development, making the demand for rapid release of MEMS sensor products, and consumer electronics in multimedia products under the influence of the growth rate is not high, the future development of the market in this area will be relatively stable. Tablet PCs in the computer field and the rapid development of a large number of applications in which the accelerometer driven the market for MEMS sensors will be worth the wait.
2011-2013 Forecast of China MEMS sensor market
The next three years, medical electronics and other products in China, production continued to maintain a rapid growth driven by China\\ s MEMS sensor market is expected to be further expanded. In addition, the emergence of new products and new applications in this market has become an important guarantee of sustainable development. 2011-2013, China\\ s MEMS sensor market will continue to maintain double-digit growth level, but in 2012, with the financial crisis led to the recovery of growth factors in decline, and market base increases, the MEMS sensor market growth rate of China will be a callback. By 2013, China\\ s sales of MEMS sensor market is expected to reach 21.42 billion yuan.
2011-2013 Analysis of China MEMS sensor market trends
Diversification of products and technology continue to promote the release of MEMS sensor market potential
Overall, MEMS sensor market more products and new products, new technologies emerging, is the most dynamic and semiconductor market segments of potential, and diverse product development not only for the development of MEMS sensors market add vitality, while also a large extent, help to reduce and disperse market risks.
Specifically on the product, the main product acceleration, pressure sensors, inkjet technology has been relatively mature first-class products and stable technology research and development mainly reflected in the indicators of performance and optimization. DMD micromirror array is better used in mobile phones and other portable devices, further scaling of their size has become a research focus. In addition to traditional products, the emergence of new products such as magnetic sensors has become a large-scale application of the overall MEMS sensor market is a major highlight. In addition, some cutting-edge products such as new MEMS oscillators, MEMS-based storage, MEMS batteries are in development stage and is expected in the next three to five years to achieve good economic returns. In addition, the product form, some of the MEMS sensor products has grown from the original single-chip modules and system solutions to upgrade to speed products to market and promote the application.
In addition to the design of MEMS sensor technology products outside, MEMS sensor technology is the product of the MEMS sensor products manufacturing industry and business critical applications. As the MEMS sensor is essentially a micro-mechanical structures, different internal structure of MEMS sensors are different, but also has many kinds of MEMS sensors, the output characteristics of small, which gives the standard MEMS sensor technology research and development to bring greater difficulty . The future, MEMS sensors will further develop production processes and MEMS and CMOS process will be further integration of MEMS sensors in order to promote the establishment of standard processes. In addition, to further reduce product cost, 8-inch MEMS sensor production line number gradually increased, and independent of the number of MEMS sensors increase foundry, but also for large-scale MEMS sensor manufacturing technology development and create a favorable environment for industrial development.
Modular and system upgrade protection products in the market to maintain price stability in heavy volume
With the MEMS sensor technology to mature and expand production, MEMS sensors will be further reduced prices. At the same time, the whole product because of the different considerations of cost control, reduction of MEMS sensors and other components of demand is relatively strong prices. Specific areas from the application point of view, 3C fastest decline in the field of MEMS sensors in 2010, used in mobile phones, laptops and other portable devices in the price of the acceleration sensor, following a substantial decrease in 2009, a decline of more than 20% again. By contrast, the field of medical electronics and other products for the whole price-insensitive, so one of the accelerometers, pressure sensors and other MEMS sensors is relatively stable price decline.
In addition, specific to the product, MEMS inkjet print head, the performance of silicon microphones and other products and applications have matured, prices have stabilized. Some new products and applications such as portable devices used in micro-mechanical gyroscopes, magnetic sensors and other products prices fell rapidly. In addition, to further enhance the profitability of the market and the establishment of the unique advantages of the product, manufacturers of MEMS sensors from simple to higher value-added supplier of MEMS sensor module and upgrade the system or solution provider, will allow a period of time the average selling MEMS sensors price rise.
“Eleventh Five” Medical Device Regulatory Review
Review of medical device regulation, \"Eleventh Five\" process, Yue Wei has strong feelings: \"This year, medical supervision is taking a start from the bottom, climbing step by step the road, though experiencing some setbacks, but still made to make people were proud of the achievements: medical devices carried out special rectification, reinforced by standards, testing technical support system for the core and build the regulatory framework for in vitro diagnostic reagents, introduced the \"Medical Device Good Manufacturing Practice\", etc. It can be said, five years, medical supervision is tempered in advance. \"
Indeed, the \"Eleventh Five-Year\" period, China\\ s medical device regulatory system to the base from the regulatory progress, from the detection system to routine monitoring, from registration to adverse events monitoring, management of all aspects of breakthrough medical device to promote the cause the pace of progress monitoring.
- The progress of laws and regulations. In 2006, \"Supervision and Regulation of Medical Devices\" revision started. 5 years, relevant departments have organized a survey of 34 key topics. In September, the State Council Legislative Affairs Office on \"Supervision and Regulation of Medical Devices (Amendment Bill)\" to the public for comments. In 2007, the State Food and Drug Administration issued an \"in vitro diagnostic reagents production implementation of the Rules (Trial)\", \"in vitro diagnostic reagent system for assessing the implementation of quality management\" and the \"in vitro diagnostic reagents for the evaluation of production quality system standards\", perfected in vitro supervision and regulation system diagnostic reagents for in vitro diagnostic reagents to enhance the production quality management system to provide a regulatory basis for the realization of the whole process of regulation, in vitro diagnostic reagents continue to promote the improvement of product quality and industrial health regulations laid a foundation. December 2009, the State Food and Drug Administration issued a \"Medical Device Good Manufacturing Practice (Trial)\" and its supporting documents and a series of normative documents for quality at the source, to achieve the final product from the regulatory supervision of the whole process change, and constantly promote the quality of medical products and medical devices to improve the healthy development of the industry laid the basis for laws and regulations.
- Standard construction progress. Past five years, the standardization of medical devices has been an unprecedented development. Before 2004, China has no standards of medical device materials. \"Eleventh Five-Year\" period, the State Food and Drug Administration successfully applied for a special state finance \"national medical device standard, standard calibration and review projects,\" the field of medical devices to create a standard material, in particular, medical laboratory and clinical testing in vitro diagnostic system of Standard Material new situation. Currently, medical devices are being developed over 20 kinds of standard materials. Among them, ethylene oxide standard material has been approved, became the first medical device approved reference material. In 2009, the global outbreak of H1N1 flu. In response to this public health emergencies, the State Food and Drug Administration and health department to establish the diagnosis of infectious diseases associated with the H1N1 influenza virus nucleic acid national reference materials, and have been approved. This is accomplished for China to establish joint prevention and control of major infectious diseases quickly laid the foundation system. This is the standardization of medical equipment in the \"Eleventh Five-Year\" period of the outstanding achievements and significant contributions. December 2009, the State Food and Drug Administration Medical Device Management Center was established standards. As of December 2009, China has issued national standards for medical device 180, the industry standard 727, covering the medical devices included in Categories 306 categories of medical device products, initially formed with a certain coverage standards.
- Register review progress. With the administrative rules and regulations of the enrichment and improvement of registration procedures, registration of medical devices approval process to change the original administrative acceptance, technical evaluation and administrative examination and approval, \"bundle\" model, to achieve the sub-management, namely, administrative acceptance, technical review evaluation and administrative examination and approval of the three separated. Work in the evaluation and approval to implement the \"three systems a\", that staff review the trial implementation of collective responsibility, to prevent the abuse of power by individuals; implement accountability system evaluation and approval, the approval of illegal acts to strengthen accountability; pre-trial assessment system and approval of inspectors to avoid publicity system; promote information technology evaluation and approval, the full implementation of online acceptance, approval online, online publicity. Implementation of sub-management, implementation of the \"three systems one of the\" registration of medical devices in order to ensure open, fair, impartial, and lay a good foundation.
- Daily monitoring of progress. There has been a long time to resolve the re-approval of light regulation, medical device manufacturers to strengthen the daily supervision, to ensure the quality of medical products, the State Food and Drug Administration in 2006 issued a revised \"day to day supervision and management of medical device manufacturing requirements.\" clear national and provincial, city and county regulatory authorities at all levels of daily supervisory duties, clear the routine supervision and inspection of the scope, focus, content, timing and frequency of supervision and inspection requirements. To strengthen the high-risk medical device manufacturer\\ s production control, the past five years, the State Food and Drug Administration has successively organized a variety of vascular stents and other key production quality management system of special inspections. In 2009, the State Food and Drug Administration organization released one after another in recent years the focus of control varieties were re-screened, reviewed, revised release of the \"National regulatory medical device directory (2009 edition)\", as the regulatory authorities at all levels to implement high-risk products provide a basis for focused regulation.
- Adverse event monitoring progress. In 2006, the State Food and Drug Administration issued a \"Circular on Further Strengthening of medical device adverse event monitoring related issues notice\", in addition to calls for further strengthening of medical device adverse event monitoring, it also proposed a medical device adverse event monitoring and recall of relevant requirements, the initial establishment of a medical device recall reporting system. December 29, 2008, \"Medical Device Adverse Event Monitoring and re-evaluation of management (tentative)\" by the State Food and Drug Administration and the Ministry of Health jointly promulgated, filled the adverse event monitoring and re-evaluation of regulatory gaps. 2005 to 2009, the state central database receives each year the number of reports of suspected adverse events were increased from 1887 to 60,305 copies, the cumulative total of 121,607 copies. As of the end of 2009, a total of 34 provincial-level implementation monitoring body, set up in parts of the city, county, township monitoring bodies, which cover the lower to monitoring bodies, 11 municipal, to cover the county (district) grade 13, to cover the township (town) level four.
In the tempered forward, in advance breakthrough. It is this all break, and constantly reinforce the medical device regulatory basis for progress. The next five years, will achieve new breakthroughs.
Medical device industry: the rapid growth of competition
Speed ??the development of industry giants looming integration
In the long term China\\ s medical device market has great potential, the current industry is the development of the critical point in the integration. And professional development in the integration process will give rise to future industry giants.
With the medical device industry
Investment highlights the following: integration of China\\ s medical device industry in the development of the critical point, the leading specialized market segments M & foster, birth merger integration industry giants. Eisai mainly from the primary start-up phase to the categories of the initial stage of expansion, to the 1990s, private capital to promote structural changes in phase, the Chinese medical device industry to complete the original technology and capital accumulation, and initial implementation of product structure adjustment and regional industry layout. Start a new medical reform in 2006, the industry entered a new historical period. Diversification strategy demands, fierce competition and capital strength to become a catalyst for industry consolidation in the industry and the health characteristics of the joint action of the external environment, enhance concentration and diversification trends form. China\\ s domestic medical device companies through mergers and acquisitions, to promote the industry to focus on. And professional development in the integration process, the emergence of more market segments leader, and gave birth to the future of the industry giants.
Future development of the strategic positioning decision, first and business expansion is expected to become industry giants. Integration period of development, China has three medical device companies will be the development of pattern choices: 1) focus on market segments, segment leading achievement; 2) expansion through mergers and acquisitions, to become integrated giants; 3) advantages of using technology to achieve Medical electrical integration. Focus and diversity are essential, we believe that diversity, and actively expand the enterprise to integrate more want to be the winner. Mindray Medical, WEIGAO [36.00-1.10%], diving medical [28.02-0.25% stock research reports it], Dunlop medical [18.28-2.51% stock research reports it] has been through joint ventures, mergers and acquisitions to diversify, become an integrated leader. Minimally invasive medical [3.45-4.17%], Comfort Medical, creation care, nine medical security [14.58-1.42% stock research reports it], Yang Pu medical [12.24-2.08% stock research reports it], Xinhua medical [33.73- 1.72% stock research reports it] is the segment leader in the field. Wandong Medical [15.290.00% stock research reports it], although only focus on one segment, but behind the development of China Resources Group carries the medical device industry expectations.
Industrial upgrading trend, China\\ s medical device industry from traditional manufacturing to high-tech development. Manufacturing process is the development of China-based medical device industry, through the accumulation of products has established a complete system, and established in the field of low-end product a pivotal position. China Medical Device actively upgrading technology for domestic market and external industrial transfer opportunities. Product quality, enhance the technological structure makes the Chinese enterprises in the care, medical imaging equipment, laboratory equipment and clinical areas such as minimally invasive treatment to obtain remarkable results. Innovation and development of an irreversible trend, computed tomography, magnetic resonance, cardiac electrophysiology devices, artificial joints will be the next occupied the high ground.
Chinese medical device market has great potential to sustain rapid growth. Global medical device industry growth than the pharmaceutical market, the future will maintain 10% -15% compound growth rate. While the developed countries accounted for 78% of the market, however, developing countries represented by China\\ s market is experiencing rapid growth, the accumulation of the cost benefits of upgrading the industrial chain and R & D position. Rising health care costs, rising health awareness and spending power will be a positive factor to promote the development of the industry, pharmaceutical industry and health system to inject additional momentum, as the release of pent-up demand, and potential future open space induced force. Rebalance the allocation of resources, upgrading and industrial transfer of internal and external dynamics are intertwined, the Chinese medical device industry compound annual growth rate will remain at 20% -30%.
Industry risk:
1) the recession, cut spending may inhibit the high-end export market demand; 2) appreciation of the renminbi to weaken China\\ s global competitiveness of manufactured products; 3) medical equipment production and sales in all countries are subject to strict regulation, policy changes could significantly improve the manufacturing costs; 4) foreign large medical device companies to accelerate into the Chinese market, domestic brands and increased competition may drive down industry profits.
Worrying gratifying sales margins
Large medical device companies will benefit from the new GMP, and infrastructure expansion. As China\\ s rising industry standards, as well as generic manufacturers from around the world (especially in India pharmaceutical companies) for cost-effective growing demand for production equipment, Xinhua medical [33.72-1.75% stock research reports it] and Tung Fu Long [45.61-0.50% stock research reports it] on the long-term major medical device companies are optimistic about growth prospects. We reiterate our positive view of Xinhua medical reasons in 2011 after the implementation of GMP in the new company\\ s profit is expected to achieve strong growth of 96.8%, also with a strong R & D capabilities, the company will continue to introduce new products and services (operating room as a whole solution).
Cost and speed of medical supplies in the market is crucial. We believe that domestic enterprises have the potential to seize market share from the hands of transnational corporations. By focusing on the domestic manufacturers are developing high-margin products (such as the shift from traditional syringes pre-filled syringe) into the upper reaches of the industrial chain. Creation of medical and minimally invasive medical [3.45-4.17%] and other companies in order to remain competitive in the bidding, is working through a range of products, rather than a single product into the joints (knee, hip) equipment market. However, due to poor product quality reputation, the market can accept the joint product of domestic concerns still remain.
Sales market is expected to grow strong, but margin pressure is a new concern factors: First, for the second half of 2011 to prepare the tender. Our research enterprise of China\\ s medical device industry, long-term growth potential of the overall positive view, because most companies believe that sales in the next 2-3 years, demand will remain strong, with an annual compound growth rate of 25-30%. However, the uncertainty of the tender (provincial policy and central policies are different) is the industry\\ s profit margin pressure facing the main policy. Our research enterprise that China may begin in the second half of 2011 high-end medical equipment and supplies for the tender at the provincial level, in order to control overall health care costs, because the Government believes that the tender price to manage areas in central and easy to supervise. Development of many new products are waiting to enter the market before the scope of the tender, and businesses are expected when the next round of bidding the price will be lowered.
The new portable device used to check diabetic neuropathy
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Canadian researchers in September, "diabetes" magazine report, a portable, automated device can accurately detect the sural nerve electrophysiological abnormalities, suggesting that diabetic sensorimotor polyneuropathy.
First author, University of Toronto BruceA.Perkins and colleagues with conventional nerve conduction study compared to assess the NC-stat System (NeuroMetrix) performance.
Dr. Perkins said, this device can have a good pre-set curved panel, neuron-specific electrodes through the panel, so the technician can be panel wrapped in patients with ankle, electrodes are placed in the correct position, without expert help. Whole process took about 5-6 minutes per patient. Other components of the device is a display of data and data from the workstation to a remote biosensor conduction system monitor call information online. Report is automatically generated, including reference data, and in about 40 minutes sent to the doctor.
They assessed the diagnostic laboratory has been completed by the professional power of conventional nerve conduction study of 72 subjects of the potential size of the sural nerve. The researchers used non-technical site inspection device repeat the test. The authors report, site inspection devices and conventional high correlation between the treatment (p <0.001). The device detects polyneuropathy 92% sensitivity and specificity of 82%.
The researchers concluded that, in the basic treatment of nerve conduction testing can reduce the damage transferred to the professional electromyography laboratory number.