• 한국건축시공학회:학술대회논문집
• /
• 한국건축시공학회 2018년도 추계 학술논문 발표대회
• /
• pp.55-56
• /
• 2018

In order to reduce the risk of accidents, we proposed a construction safety management system combined with wearable device and LoRa (Low-Range Wireless Network) communication method to apply the usefulness of Internet (IoT) technology which means "everything connected". to construction safety management Management system. The proposed wearable safety device is a device that relays information exchange between wearable safety device and safety management server by LoRa wireless communication method. The safety management server can store workers bio-data and perform big data analysis. If a risk factor is determined from the analysis result, a warning is sent to the wearable safety device and the manager's application. The goal of this system is to prevent construction workers from entering the dangerous area that is not suitable for work, and to prevent safety accidents caused by human cause by detecting abnormal condition during work.

• 융합보안논문지
• /
• 제11권4호
• /
• pp.67-75
• /
• 2011

최근 많은 외산제품들이 국내시장에 유입되고 국내 제품의 출시로 스마트폰 사용자는 급속히 증가하고 있다. 스마트폰 사용자가 증가함에 따라 모바일 악성코드 또한 빠르게 증가하고 있다. 이에 모바일 악성코드에 대한 적절한 대응의 필요성이 증대되고 있다. 단말 관리 방법으로는 SNMP, TR-069 프로토콜이 널리 사용되었지만 이들 프로토콜은 제한적인 관리기능, 이동성 미지원 등으로 인해 모바일 단말 관리에는 적합하지 않다. 모바일 단말 관리 표준인 OMA DM 프로토콜이 대부분의 2G, 3G 무선 단말들의 관리 프로토콜로 채택되고 있으며, 따라서 스마트폰 단말 관리를 위해서도 적합한 프로토콜이라 할 수 있다. 본 논문에서는 악성코드에 대한 현황을 설명하고 스마트폰의 악성코드를 원격제어로 제거할 수 있는 OMA DM기반의 단말 관리 시스템을 설계하였다.

• 대한의용생체공학회:의공학회지
• /
• 제44권2호
• /
• pp.99-108
• /
• 2023

According to the COVID-19, development of various medical software based on IoT(Internet of Things) was accelerated. Especially, interest in a central software system that can remotely monitor and control ventilators is increasing to solve problems related to the continuous increase in severe COVID-19 patients. Since medical device software is closely related to human life, this study aims to develop central monitoring system that can remotely monitor and control multiple ventilators in compliance with medical device software development standards and to verify performance of system. In addition, to ensure the safety and reliability of this central monitoring system, this study also specifies risk management requirements that can identify hazardous situations and evaluate potential hazards and confirms the implementation of cybersecurity to protect against potential cyber threats, which can have serious consequences for patient safety. As a result, we obtained medical device software manufacturing certificates from MFDS(Ministry of Food and Drug Safety) through technical documents about performance verification, risk management and cybersecurity application.

• 품질경영학회지
• /
• 제46권2호
• /
• pp.211-224
• /
• 2018

Purpose: It can easily be understood that more rules and regulations need to be imposed on the medical device industry due to its impact on public health and hygiene. Domestic medical device manufacturers are thus required to comply with the requirements specified in the good manufacturing practice (GMP) system, and it is essential to abide by the international standards as well to sustain their global competitiveness. The main purpose of this study is to review the guidelines of the medical device GMP system in Korea and propose future directions for further enhancement of the GMP system. Methods: Specific requirements prescribed in international standards, such as ISO 9001:2015, ISO 13485:2016, ISO 14971:2012, and ISO 14155:2011, are analyzed and compared with the domestic GMP system. Results: It has been observed that the generic international standard related to quality management system, ISO 9001:2015, lays out the foundations for the development of quality management system relevant to medical device industry, ISO 13485:2003, with which the domestic GMP system is fully compatible. Further, several important aspects of risk management and clinical trials of medical devices are also recognized and included in the domestic medical device GMP system. Conclusion: Even though specific requirements of individual ISO standards are slightly different from each other, their overall structure and framework may contribute to the development and enhancement of globally competitive GMP system of the domestic medical device industry.

• Journal of Information Processing Systems
• /
• 제13권6호
• /
• pp.1459-1466
• /
• 2017

Recently, the development of the smart home field provides a range of services to install and keep the smart home appliance in a user's residential environment pleasantly. However, the conventional system method is not convenient enough to use properly because users have to select a device and manually operate the device on their own. In this paper, we propose a system to set the priority of the devices selected by the user and proceed with the task. When a user selects a device, the system recommends an optimal device associated with the device. The system compares and sets the priority of each device, carrying out the task one by one according to the set priority. Therefore, the proposed system is expected to provide users with increased convenience and more efficient task management.

• 한국정보통신학회:학술대회논문집
• /
• 한국해양정보통신학회 2007년도 춘계종합학술대회
• /
• pp.645-648
• /
• 2007

본 논문은 모바일 장치에 의한 데이터베이스 관리 시스템에 관해 기술한다. 본 시스템은 모바일 장치를 사용해서 언제 어디서든지 즉시 원격으로 데이터베이스를 관리 가능하다. 이를 위해 모바일 디바이스와 인터페이스 가능한 dataset server CE와 모바일 장치에서 운용 가능한 데이터베이스 관리 시스템 및 모바일 장치를 데스크톱 컴퓨터와 연결 시켜주는 웹 서비스 프로그램을 개발했다. 외부의 모바일 장치는 웹 서비스 기능과 무선으로 연결한다. 개발한 시스템은 dataset server CE 클라이언트 엔진, 웹 서비스 서버 에이전트 및 모바일 관리 시스템을 포함한다. 애플리케이션 프로그램을 이용해서 시스템의 기능을 테스트 했고, 테스트 결과 개발한 시스템이 원래의 목적대로 잘 운용됨을 확인했다.

• 대한의용생체공학회:의공학회지
• /
• 제44권1호
• /
• pp.41-52
• /
• 2023

With the international change in the medical device market owing to the development of innovative medical engineering and the use of various raw materials, a systematic and rational medical device classification system is needed to safely manage newly developed medical devices. This study aims to improve the domestic medical device classification system by proposing product establishment and segmentation. It is based on medical device products from the United States and Europe that are only available in foreign systems and are more subdivided than domestic products. This study analyzes and compares the domestic and foreign medical device classification systems by examining laws, guidelines, and analysis reports in Korea, the United States, and Europe. In accordance with product establishment and segmentation criteria, products subject to improvement are presented. This study contributes to safely managing medical devices that do not fit with the current classification system and to solving the confusion caused by the lack of international harmony in product classification systems.

• 한국항행학회논문지
• /
• 제12권1호
• /
• pp.15-21
• /
• 2008

본 논문에서는 관리대상자의 위치 및 기타 관련 정보를 위치관리시스템(LMS : Location Management System)에서 항시 감시 및 관리할 수 있는 GPS 기반 위치 인식 단말시스템 및 위치관리시스템을 구현하였다. 구현한 시스템은 PID(Personal Identification Device)의 정보를 전송하기 위한 모듈과 GPS 기반의 위치정보 수집 모듈로 구성된 위치 인식 단말장치 (Mobile HTE : Mobile Home Terminal Equipment)와 Mobile HTE에서 수신된 정보를 인터넷 망을 통하여 위치관리시스템에 전송할 수 있는 단말장치 (HTE : Home Terminal Equipment)를 구현하여 관리대상자의 위치를 관리할 수 있는 위치관리시스템을 설계 하였다.

• 대한의용생체공학회:의공학회지
• /
• 제44권1호
• /
• pp.73-79
• /
• 2023

The purpose of this study is to derive medical devices with different management systems through comparison of domestic and overseas medical device product classification systems and to propose management conversion measures for the products. The definitions of medical devices were compared and the scope of medical devices defined by each country was confirmed through surveys of the Medical Device Act, Federal Food, Drug & Cosmetics Act (FD&C) in the U.S., and Medical Device Regulations (MDR) in Europe. Using the Ministry of Food and Drug Safety's regulations on medical device products and grades, 21 CFR part 860-892 and product code classification files in U.S., and EMDN in Europe as basic data to compare medical device products and derive medical devices with different management systems. As a result of comparing the definition and product classification systems of medical devices in Korea, the U.S. and Europe, medical device accessories, prosthetic limbs and aids among assistive devices for persons with disabilities, drugs, quasi-drugs and industrial products that are not managed by medical devices in Korea are managed as medical devices in the U.S. and Europe. This study aims to improve public health by securing systematic product safety management and essential performance under medical device regulations. Management within a single medical device system will increase the efficiency of licensing work of domestic medical device manufacturers and related organizations. It is also expected to help advance the system according to the international harmony of the item classification system and enhance smooth import and export competitiveness.

• 교육녹색환경연구
• /
• 제9권3호
• /
• pp.1-11
• /
• 2010

In the construction industry, IT based information system has been diversely applied to increase productivity. Although IT device such as PDA, RFID, Barcode, wireless network and web camera has been introduced to gather information in construction site, the effect of the IT device is limited, because of bringing about additional works of engineer. In this paper, we proposed a defect management system which is based on handwritten document digitalization framework for introducing applicability of new IT device, digital pen. By the proposed system, we can effectively gather and input defect information to defect management system by using digital pen and paper like conventional way. Applying the data gathering device, digital pen to defect management, it is able to increase productivity by improving work process, building up and utilizing defect information database of good quality.