Quality Control of Camouflage Materials Research Based on C2GS2 Model

2014 ◽  
Vol 644-650 ◽  
pp. 4814-4818
Author(s):  
Ling Li ◽  
Jun Liu ◽  
Xu Liang Lü ◽  
Ming Xu Sui ◽  
Guo Jing Wu ◽  
...  

In view of the problems in the process of camouflage materials research and development project quality control subjective and management information of materials is unilateral, C2GS2 quality control model was built to improve the scientific management level. By the establishment of index system for quality control, on the basis of the characteristics of its all output index, output-CCR model was set up to evaluate the management level. In order to further improve the information of both radial direction and non-radial detection, we introduced the non-Archimedean infinitesimal to form C2GS2 quality control model. The example shows that the quality control model can significantly improve the level of research and development, it can provide more detailed manage information.

2014 ◽  
Vol 644-650 ◽  
pp. 4705-4709
Author(s):  
Jun Liu ◽  
Ling Li ◽  
Xu Liang Lv ◽  
Xiao Di Weng ◽  
Zheng Zhou

The proposed super-efficient C2GS2 quality control model in this article aims at simplifying the assessment of efficient C2GS2 decision making units (DUMs) during the process of quality control in camouflage materials project development. Firstly, based on the establishment of quality control index system, DUM itself are removed in reference set. Then DUMs could be sufficiently ranked, according to the compare among every DUM itself and other ones’ linear combinations. Simultaneously, projections of C2GS2 quality control model are analyzed to complement the super-efficient theories and several experimental examples are provided.


2015 ◽  
Vol 733 ◽  
pp. 968-973
Author(s):  
Jian Wei Feng

In order to improve the inherent safety management level of equipment complex system, based on the fact that present study of inherent safety management ignore the harmonious alternating function between system microcosmic elements, analyzed the basic theory of system harmonious alternating mechanism, put forward a more perfect SHELLOM model, then set up an equipment safety degree model based on harmonious alternating mechanism. After the Definition of inherent safety management, constructed the risk early control model and human safety performance control model of inherent safety management system, and analyzed the safety cost and safety benefit, put forward the notion of safety culture radiation, narrated the relation of safety radiation effect and system harmonious alternating mechanism, provide effective reference for the construct of equipment complex system inherent safety management.


2014 ◽  
Vol 496-500 ◽  
pp. 2265-2268 ◽  
Author(s):  
Ping Li

In this paper, the actual situation of university management and the specific needs of colleges and universities to study and design a set of management information systems. Management information so that the original approach gradually to computers and computer networks as the carrier of the campus electronic information processing and transmission replaced, through the network, the use of multimedia and communication technologies for remote teaching, faculty achieve complementarity. Achieve scientific management, modernization; use of modern means to improve the quality of teaching and management level


2015 ◽  
Vol 3 (2) ◽  
pp. 1-7 ◽  
Author(s):  
Achin Jain ◽  
M P Venkatesh M P ◽  
Pramod T.M. Kumar

In Tanzania, Tanzania Food and Drugs Authority (TFDA), is a regulatory body responsible for controlling the quality,safety and effectiveness of food, drugs, herbal drugs, cosmetics and medical devices. The Authority has been ensuringsafety, efficacy and quality of medicines by quality control tests; in addition to other quality assessment mechanisms.The guidelines laid by TFDA have also emanated from commitment to democracy and gives strong emphasis to thefulfilment of the needs of the less privileged rural population.Tanzania is an emerging market; the pharmaceutical market is valued at over US$250 million, and is growing at anannual rate of around 16.5% and is expected to reach approximately US$550 billion in 2020. Currently, the market ishighly dependent on imports, which account for around 75% of the total pharmaceutical market.The procedures and approval requirements of new drugs, variations, import, export and disposal have been set up bythe TFDA, which help in maintaining quality of the drug products that are imported as well being produced locally 


2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Qunying Mao ◽  
Miao Xu ◽  
Qian He ◽  
Changgui Li ◽  
Shufang Meng ◽  
...  

AbstractThe outbreak of COVID-19 has posed a huge threat to global health and economy. Countermeasures have revolutionized norms for working, socializing, learning, and travel. Importantly, vaccines have been considered as most effective tools to combat with COVID-19. As of the beginning of 2021, >200 COVID-19 vaccine candidates, covering nearly all existing technologies and platforms, are being research and development (R&D) by multiple manufacturers worldwide. This has posed a huge obstacle to the quality control and evaluation of those candidate vaccines, especially in China, where five vaccine platforms are deployed in parallel. To accelerate the R&D progress of COVID-19 vaccines, the guidances on R&D of COVID-19 vaccine have been issued by National Regulatory Authorities or organizations worldwide. The Center for Drug Evaluation and national quality control laboratory in China have played a leading role in launching the research on quality control and evaluation in collaboration with relevant laboratories involved in the vaccine R&D, which greatly supported the progression of vaccines R&D, and accelerated the approval for emergency use and conditional marketing of currently vaccine candidates. In this paper, the progress and experience gained in quality control and evaluation of COVID-19 vaccines developed in China are summarized, which might provide references for the R&D of current and next generation of COVID-19 vaccines worldwide.


Plants ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 466
Author(s):  
Marie-Christine Carpentier ◽  
Cécile Bousquet-Antonelli ◽  
Rémy Merret

The recent development of high-throughput technologies based on RNA sequencing has allowed a better description of the role of post-transcriptional regulation in gene expression. In particular, the development of degradome approaches based on the capture of 5′monophosphate decay intermediates allows the discovery of a new decay pathway called co-translational mRNA decay. Thanks to these approaches, ribosome dynamics could now be revealed by analysis of 5′P reads accumulation. However, library preparation could be difficult to set-up for non-specialists. Here, we present a fast and efficient 5′P degradome library preparation for Arabidopsis samples. Our protocol was designed without commercial kit and gel purification and can be easily done in one working day. We demonstrated the robustness and the reproducibility of our protocol. Finally, we present the bioinformatic reads-outs necessary to assess library quality control.


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