• Journal of the Korean Society of Propulsion Engineers
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• v.22 no.4
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• pp.117-124
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• 2018

USA and Europe are leading the transport airplane industry. In Asia-Pacific region, air transportation and MRO industries are forecasted to be grown up rapidly. Furthermore, Japan and China entered into design and manufacture state of regional airplane, while developing countries entered into severe struggle competition for MRO industry. Global aircraft MRO and engine MRO industries are forecasted 3.4% and 7% annual growth respectively in the next decade. In this paper, authors propose promotion strategy for technology intensive MRO of aircraft engine to create a higher value-added business.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.22 no.3
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• pp.310-315
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• 2021

In the case of weapon systems used by the military, defense standards are applied for economical and efficient procurement, management, and maintenance. Defense specifications are documents describing procedures and methods for determining whether technical requirements for products and services are consistent and apply to the production of weapon systems, quality assurance, and configuration management. Software is also subject to defense specifications, and is documented and managed in the same way as other defense specifications. Sometimes it happened to be standardized without some(or all) software. In this case, a competitive contract is impossible and it may affect the quality of weapon systems because the manufacturer arbitrarily changes the software without prior approval. So, software standardization is required, but it is very difficult to verify for firmware installed in hardware. This paper proposed a verification method for g software standardization, and we expect it will contribute to the efficient production and quality assurance of weapon systems.

• Journal of Advanced Navigation Technology
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• v.28 no.5
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• pp.670-677
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• 2024

In this study, the flight test measurement data and flight test items for metal-based brake pads for transport aircraft were derived through the analysis of Korea and the U.S. aviation-related regulations, technical standards and airworthiness standards. During the flight test, the measurement items should be measured at all times, such as aircraft altitude, speed, aircraft condition, wind direction, wind speed, and air-temperature. The flight test items of the brake pad should be quantitatively evaluated for stopping performance during landing, fuse plug integrity, stopping performance at reject take-off situations, anti-skid compatibility during landing and parking brake capability. Additionally, qualitative evaluation of the flight test pilot's aircraft steering characteristics under each test condition is required. The identification of risk factors for each test item and measures to mitigate risk factors must be approved in advance before the flight test, and the risk factors must be reevaluated to maintain suitability for the flight test during the flight test, and the results must be documented.

• Journal of Biomedical Engineering Research
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• v.31 no.6
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• pp.434-437
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• 2010

For approval of medical devices manufactured or imported, submission of technical documents as well as the application form is required. The manufacturer (or importer) should properly identify the raw materials the applied product is made of and the manufacturing processes the product undergoes before it is shipped in the application form. In the technical documents, scientific data to evaluate the efficacy, safety, and quality of the applied product that has been described in the application form should be provided. Therefore, identifying the raw materials that were used for the parts of the applied product and describing the physical and chemical characteristics of the raw materials are quite important and essential in ensuring the efficacy, safety, and quality of the applied product. To describe the physical and chemical characteristics of the raw materials correctively, the applicant is required to have broad knowledge in the scientific fields such as chemical, polymer, metal, and ceramic science and engineering. But most of the applicant are not experts in these fields, so that the description in the application form often includes wrong and improper descriptions. Thus, we developed a guideline which explains the raw materials for medical devices, show the their examples. The purpose of this description guideline is to help the applicant properly completing the "Raw materials or constituents and their volumes" part in the application form.