• 화약ㆍ발파
• /
• 제32권1호
• /
• pp.23-30
• /
• 2014

국내 화약류에 대한 전반적인 관리와 발파작업에 대한 규정은 총포 도검 화약류등 단속법에 의하여 관리되고 있으나, 세부적인 취급과 사용법에 대한 지침은 산업안전보건법 제27조에 의거하여 발파작업 표준 안전작업지침을 마련하여 발파작업에서의 재해예방을 위한 화약류의 취급, 운반, 저장, 사용 및 관리와 작업상의 안전에 관하여 사업자에게 지도 권고하고 있다. 본 연구에서는 고용노동부에서 고시한 발파작업 표준 안전작업지침에 대하여 검토하였고, 국내화약시장에 도입된 신제품과 최신발파기술이 지침의 개정 시 반영될 수 있도록 화약류에 대한 용어의 정의와 추가로 포함해야 하는 에멀젼계 폭약과 벌크형태의 폭약, 그리고 최근 국내 발파현장에서 사용이 증가하고 있는 전자뇌관에 대하여 수록을 제안하였다. 또한, 작업지침에 대해서는 비전기식 뇌관과 전자뇌관의 대표적인 취급 방법을 예시를 들어 제안하여 지침안 개정 시 보완된 발파작업 표준 안전작업지침을 마련하도록 제안하였다.

• 대한안전경영과학회지
• /
• 제11권4호
• /
• pp.177-191
• /
• 2009

In this study, we suggest a standardization of the logistics terminologies in Korean Standard to improve its consistency. To support this work, some principles for terminology selection and corrections are studied based on the guideline in international standard. The revised terminologies are summarized in Appendix for 20 logistics-related Korean Standards.

• 한국산업보건학회지
• /
• 제31권4호
• /
• pp.385-395
• /
• 2021

Objectives: This study aimed to select items for technical guidelines through the guidelines of the Korean Occupational Safety and Health Agency (KOSHA) for agricultural workplaces. Methods: All 1,308 guidelines provided by KOSHA were reviewed and categorized using a Delphi technique questionnaire on their compatibility and urgency. Results: Among all the KOSHA guidelines, 100 items related to agricultural workplaces were selected. After that, two Delphi questionnaires were conducted and 46 items were finally selected. The average compatibility was calculated as 4.26, and urgency was 2.39. As a result of measuring the content validity of 46 items, six items were identified that were not relevant to agriculture. The final selected items were classified into four categories: Health examination and management, machinery standards, safety and health standard guides, and workplace environment management. Conclusions: The various risk factors at agricultural workplaces should be prevented and managed. It was shown that related technical guidelines or work standard manuals should be prepared. The technical guidelines of KOSHA will be provided as basic categories in the agricultural sector.

• 대한의용생체공학회:의공학회지
• /
• 제40권5호
• /
• pp.197-205
• /
• 2019

The existing Extracorporeal membrane oxygenation(ECMO) and Cardiopulmonary bypass system(CPB) have been developed and applied to various devices according to their respective indications. However, due to the complicated configuration and difficult usage method, it causes inconvenience to users and there is a risk of an accident. Therefore, smart all-in-one cardiopulmonary circulation device is being developed recently. The smart all-in-one cardiopulmonary assist device consists of a blood pump for cardiopulmonary bypass, a blood oxidizer for cardiopulmonary bypass, a blood circuit for cardiopulmonary bypass, and an artificial cardiopulmonary device. It is an integrated cardiopulmonary bypass device that can be used for a variety of purposes such as emergency, intraoperative, post-operative intensive care, and long-term cardiopulmonary assist, combined with CPB used in open heart surgery and ECMO used when patient's cardiopulmonary function does not work normally. The smart all-in-one cardiopulmonary assist device does not exist as a standard and international standard applicable to advanced medical devices. Therefore, in this study, we will refer to the International Standard for Blood Components, the International Standard for Blood, the Guideline for Blood Products, and prepare applicable performance and safety guidelines to help quality control of medical devices, and contribute to the improvement of the health of people. The guideline, which is the result of conducted a survey of the method of safety and performance test, is based on the principle of all-in-one cardiopulmonary aiding device, related domestic foreign standards, the status of domestic and foreign patents, related literature, blood pump(ISO 18242), blood oxygenator (ISO 7199), and blood circuit (ISO 15676) for cardiopulmonary bypass.The items on blood safety are as follows: American Society for Testing and Materials ASTM F1841-97R17), and in the 2010 Food and Drug Administration's Safety Assessment Guidelines for Medical Assisted Circulatory Devices. In addition, after reviewing the guidelines drawn up through expert consultation bodies including manufacturers / importers, testing inspectors, academia, etc. the final guideline was established through revision and supplementation process. Therefore, we propose guidelines for evaluating the safety and performance of smart all-in-one cardiopulmonary assist devices in line with growing technology.

• 한국안전학회지
• /
• 제33권1호
• /
• pp.73-80
• /
• 2018

According to the statistics publication of KOSHA, more than half of serious accidents at the construction sites were related to the temporary works and/or the temporary structures such as scaffoldings, shores, earth retaining walls, etc. The structural failures are occurred because of the overload acting on the structures or lack of performance of the one or more members of the structures. For the prevention of the collapse accidents relating to the temporary structures at the construction sites, we have to control construction processes not to occur the overload and also to control the performance and quality of each member of the temporary structures. MOLIT has amended the "Construction Technology Promotion Act" on Jan. 7th, 2015 to ensure the structural safety of the temporary structures. According to the Act, the designers of the construction design projects should check the structural integrity of the structures including the temporary structures and the construction companies have to let 'the Relative Professionals' confirm the structural integrity of temporary structures, the shores(${\geq}5m$ high) and the scaffolds(${\geq}31m$ high), before construction. Also, MOLIT has amended the "Regulation for Construction Technology Promotion Act" on Jul. 4th, 2016 for quality management and testing of temporary equipments. According th this regulation, the construction companies and supervisors should manage and test the temporary equipments before using them. In this paper, the standard drawings of the shores(< 5 m high) and the scaffolds(< 31 m high) and the amended "Business Guideline for Quality Management of Construction Work" are presented. As the result of this study, MOLIT noticed the amended "Business Guideline for Quality Management of Construction Work" on Jul. 1st, 2017.

• 한국건축시공학회:학술대회논문집
• /
• 한국건축시공학회 2021년도 봄 학술논문 발표대회
• /
• pp.247-248
• /
• 2021

Recently, the government is pursuing to reduce the serious accidents in most industries, including the construction industry, by enacting laws on punishment. The accident rate tends to be depended on the size and type of construction sites, and the accidents occur frequently due to inadequate implementation of safety management system and management standards, especially, in small and medium-sized sites. This study has performed the profiling of 265,000 accident cases on construction sites by attribute analysis such as the ratio of days lost to work, and pattern of days lost to work compared to the size of the construction. It turned out that the proportion of accident cases was high mainly in small-scale construction sites, and long-term labor losses occurred. Shortly, it is necessary to establish an institutional standard for applying a realistic safety management cost calculation and management system centered on small-scale sites. Therefore, this study is expected to be used as fundamental data or guideline for developing a customized safety management and accident prevention system for a worker reflecting the conditions of a construction site in the future.

• 핵의학기술
• /
• 제21권2호
• /
• pp.13-27
• /
• 2017

국내 의료용 방사성폐기물 자체처분과 관련하여 심사과정에서 많은 보완을 거치게 되고, 이 과정을 통과함에 많은 어려움을 겪고 있다. 이에 따라 의료용 방사성폐기물의 자체처분시 기본적인 가이드라인을 제시함으로써 의료기관의 방사성 폐기물 처리효율을 높이고자 한다. 2015년부터 2016년까지 국내 15개 의료기관의 의료용 방사성폐기물 자체처분 절차서 및 계획서 작성 시 보완 요청된 사항들을 비교 검토하였으며, 이와 관련하여 원자력 안전법 관련 규정을 기준으로 방사성폐기물 자체처분 시 서류작성에 필요한 세부 작성안 들을 도출하였다. 한국원자력안전기술원의 대표적인 보완요청사항들로는 비가연성 폐기물의 처분방법, 자체처분 예정 폐기물의 저장방법, 폐기물 자체처분의 정당성 및 자체처분 전 조치사항, 배기필터의 기준방사능 및 보관기간 산출, 폐기물 수량 측정 용기 보유 여부 및 증빙자료, 감마카운터 사용 시 측정효율 증명자료 첨부임을 확인할 수 있었다. 또한 의료 방사성 폐기물 자체처분 가이드라인 구축을 통해 방사성동위원소 핵종 및 발생유형별 분류기준 등을 명확히 제시하였다. 이를 통해, 자체처분 서류 작성에 따른 시간의 단축과 업무대행 지출비용이 발생되지 않음을 확인할 수 있었고 방사성 폐기물의 장기간 보관에 따른 보관시설의 저장효율이 좋아지고 경제적 비용도 절감됨을 알 수 있었다. 본 가이드라인을 바탕으로 방사성폐기물 자체처분의 실무적인 어려움을 겪고 있는 관계자들의 업무효율 향상에 기여할 것으로 사료된다.

• 한국철도학회:학술대회논문집
• /
• 한국철도학회 2011년도 정기총회 및 추계학술대회 논문집
• /
• pp.1624-1630
• /
• 2011

Currently the train operating environment to affect track irregularity is changed rapidly such as speed-up, linear improvement and rolling stack upgrade. The recent track maintenance criteria of track irregularity was quoted from past Japan's, and the needs of revision of criteria are increased because of the rapid change in train operating environment. In case of enhance the track irregularity criteria, it secure driving safety and riding comfort but maintenance cost are increase. And also decrease ballast durability by frequent corrective work. In case of mitigate the criteria, it decrease driving safety and riding comfort, but save the maintenance cost. The study for enacting rational criteria did not carry out so far. In this study, survey the domestic and international track irregularity and case study for track irregularity inspection results and maintenance history for guideline of enacting irregularity criteria study.

• 대한인간공학회지
• /
• 제32권4호
• /
• pp.321-331
• /
• 2013

Objective: The aim of this study is to review the literatures on the regulation, standard and guideline for the human vibration in Korea and other countries. Background: This review can be used to prevent various diseases caused by the human vibration as a basis for the development of the policy. Results: In Korea, the general employers' duties related to human vibration are set forth the Health Measures(Article 24) in the Occupational Safety and Health Act. And then an employer shall take measures to protect the health of the workers concerned by improving other working conditions relating to working hours for the vibration prevention measures referred to in Article 24 of the Act. The European Union adopted a Directive in 2002 on minimum requirements for the health and safety of workers exposed to vibration. New Regulations on Vibration at Work will be introduced in Great Britain on 2005 to implement the Directive. In the U.S., both ANSI and ACGIH adopted the ISO standard for measurement and suggested exposure action and limit values. In Japan, the Ministry of Labor decided that the vibration syndrome among operators of rock drills and riveters etc. could be included in an occupational disease(1947). In addition, ISO standard was based on proposals and draft documents of many countries such as U.K, Japan and European, etc. Conclusion: In Korea, Occupational Safety and Health Act prevent vibration to health, but do not include exposure limits. It is therefore important to consider the new duties regarding to vibration risks added to the general duties.

• 의료ㆍ복지 건축 : 한국의료복지건축학회 논문집
• /
• 제22권3호
• /
• pp.7-15
• /
• 2016

Purpose: As medicare services have gotten spreaded, clinical laboratory has been dominant position. So, it has been acted for quality control and clinical pathology accreditation. But there has been quite deficient information to evaluate working space and technical standards of medical laboratory for accreditation. This study goals to figure out accreditation standard and design guideline for clinical laboratory, and to give safe and efficient design information. Methods: This study has been searched by literature for accreditation standards and design guidelines of clinical pathology in USA, UK, and Germany. Results: Three countries have accredited based on working lab space, staff space, storage space, patient space and health and safety equipment. Design guidelines of three countries commonly have focused on worktable layout, worktable distance and module, and specific laboratory biosafety level. And USA guidelines stress on the architectural design such as design process and passage distance for escape, UK stress on the efficiency as functional work flow and construction cost, lastly Germany design guidelines stress on the operator's safety distance and workstation. Three countries have not only accreditation standards but also design guidelines for more specific quality management, separating from accrediting institute. Implications: In korea, it has been needed to make clinical laboratory design guideline for the safe and efficient environment and reliable and competitive medical service.