• Proceedings of the Korean Society of Precision Engineering Conference
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• 2005.10a
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• pp.43-48
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• 2005

In order to facilitate technical exchange among nations and/or institutes through the establishment of mutual recognition and the reliability guarantee of testing results by testing standards standardization, the interlaboratory comparison tests on brake discs and linings between KRRI and CARS were conducted. So far, two ways of comparison tests were performed for a better understanding of mutual recognition and standardization in railroad brake linings between Korea and China. In this paper, the first and second comparison testing results have been summarized, and the suggestions for the future research work are also presented to encourage extensive research on comparison study of railroad brake discs and linings between KRRI and CARS. Eventually, the final goal of the current research will be the establishment of standardization of railroad testing standards.

• Korean Journal of Veterinary Research
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• v.57 no.2
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• pp.71-78
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• 2017

Well-established standards and specifications for medical devices not only provide clarity and consistency in licensing processes but also secure device safety and effectiveness. This study reviewed regulatory standards and specifications for veterinary medical devices in Korea based on data obtained through analyses of those medical devices. General standards for electromechanical, electromagnetic, and biological safety and individual standards for 76 electric and 70 general medical device products have been established by the Korean Ministry of Food and Drug Safety. However, the first standards and specifications for veterinary medical devices were established in March 2000 for two products (disposable needle and syringe). Similar to the large number of standards for medical devices, there have been general standards for safety and individual standards for 72 veterinary medical devices (27 electric medical devices, 12 non-electric medical devices, 10 medical supplies, and 23 other types) established since 2014. These new standards considered, among other aspects, the devices' applications, usage characteristics, and industrial environment. To date, the establishment of standards and specifications for veterinary medical devices remains limited. This study suggests that improvements should be made to the regulation of general and individual standards associated with various veterinary medical instruments, supplies, and in vitro diagnostic medical reagents.

• The Magazine of the IEIE
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• v.30 no.6
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• pp.624-637
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• 2003

CMVP(Cryptographic Module Validation Program) validates cryptographic modules to FIPS 140-1, 2, and other FIPS cryptography based standards. This paper gives an overview of the CMVP, cryptographic modules, cryptographic algorithms, and the applicable standards. This provides a brief overview of the security requirements that must be met by each cryptographic module that is submitted to a CMT laboratory for conformance testing and describes the Cryptographic Algorithm Testing.

• Journal of the Korean Society for Nondestructive Testing
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• v.25 no.5
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• pp.400-404
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• 2005

• Annals of Clinical Microbiology
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• v.21 no.4
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• pp.69-74
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• 2018

Laboratory medicine is a specialized division that supports physicians in the care of patients by providing rapid and accurate in vitro diagnostic tests. Standardization of every component of a specific test is essential for producing accurate results. The Clinical and Laboratory Standards Institute (CLSI) was founded to develop a formal consensus process for standardization in 1968, and has been publishing standards and guidelines covering all aspects of clinical, research, and other laboratory work. CLSI guidelines are widely used around the world for standardization. The CLSI antimicrobial susceptibility testing subcommittee (AST SC) consists of 6 standing and many ad hoc working groups. Members of the AST SC review submitted proposals and suggestions, decide on approving these submissions in face-to-face meetings held twice a year, and revise CLSI documents accordingly. As these face-to-face meetings are open to anyone who registers to attend, I strongly encourage the members of our Society to attend and actively participate in document development.

• Journal of the Korea Institute of Information Security & Cryptology
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• v.11 no.6
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• pp.67-76
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• 2001

In this paper, we investigate criteria for evaluating cryptographic strength based on randomness testing of the advanced encryption standard candidates, which have conducted by NIST(National Institute of Standards & Technology). It is difficult to prove that a given cryptographic algorithm meets sufficient conditions or requirements for provable security. The statistical testing of random number generators is one of methods to evaluate cryptographic strength and is based on statistical properties of random number generators. We apply randomness testing on several cryptographic algorithms that have not been tested by NIST and find criteria for evaluating cryptographic strength from the results of randomness testing. We investigate two criteria, one is the number of rejected samples and the other is the p-value from p-values of the samples.

• Journal of the Korea Institute of Information Security & Cryptology
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• v.14 no.4
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• pp.3-11
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• 2004

The XML has been becoming a basis of the related application and industry standards with proliferation of electronic transactions on the web, and the standardization on XML Signature, which can be applied to the digital contents including XML objects from one or more sources, is in the progress through a joint effort of W3C(World Wide Web Consortium) and IETF(Internet Engineering Task Force). Along with this trend, the development of products implementing XML Signature has been growing, and the XML Signature products are required to implement the relevant standards correctly to guarantee the interoperability among different XML Signature products. In this paper, we propose a conformance testing method for testing the XML Signature products, which includes a testing procedure and test cases. The test cases were obtained through analysis of XML Signature standards. Finally we describe the design and uses of our XML Signature conformance testing tools which implements our testing method.

• International Journal of Stem Cells
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• v.17 no.2
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• pp.147-157
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• 2024

The objective of standard guideline for utilization of human lung organoids is to provide the basic guidelines required for the manufacture, culture, and quality control of the lung organoids for use in non-clinical efficacy and inhalation toxicity assessments of the respiratory system. As a first step towards the utilization of human lung organoids, the current guideline provides basic, minimal standards that can promote development of alternative testing methods, and can be referenced not only for research, clinical, or commercial uses, but also by experts and researchers at regulatory institutions when assessing safety and efficacy.

• Transactions of the Korean Society of Mechanical Engineers A
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• v.36 no.9
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• pp.1053-1057
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• 2012

In this study, the temperature-dependency of the tensile properties of a glass fiber reinforced plastic (GFRP) used in wind turbine blades was examined. The tensile strength, elastic modulus, and Poisson's ratio of the tensile specimen manufactured from uniaxial ($0^{\circ}$) and triaxial ($0/{\pm}45^{\circ}$) laminate composite plates were measured at four different testing temperatures-room temperature, $-30^{\circ}C$, $-50^{\circ}C$, and $60^{\circ}C$. It was found that the tensile strengths and elastic moduli of the uniaxial laminates were greater than those of the triaxial laminates over the testing temperature range. The tensile strength of the two laminates was significantly dependent on the testing temperature, while the dependency of the elastic modulus on the temperature was insignificant. Furthermore, it could be considered that the Poisson's ratio changed slightly with a change in the testing temperature.

• Analytical Science and Technology
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• v.26 no.3
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• pp.165-173
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• 2013

To establishment of PT Program for Indoor air quality field that manufacture of confidential development PTMs (proficiency testing materials) and examined of proficiency testing evaluation included sampling process whether or not that is valid. Confirmation of homogeneity and stability of PTMs prepared. PTMs were confirmed to be homogeneous enough to be used as proficiency testing materials since withinbottle homogeneities of the RMs were lower than 0.3 times of targeted standard deviation of proficiency testing. The result of this study showed that the Robust RSD of proficiency testing for VOCs (volatile organic compounds) appeared 23~43% in concentration of 50~320 ${\mu}g/m^3$ for Method A(Distribution by adsorption in Tenax-tube of VOCs), but less 13~42% in concentration of 200~1200 ${\mu}g/m^3$, 16~31% in concentration of 100~450 ${\mu}g/m^3$ for Method B (distribution by VOCs of gas phase in 10L Tedalr bag), C (directly sampling of cylinder with high pressure) respectively. The result of this study showed that method C with sampling is most adequate to the proficiency testing for VOCs in indoor air.