• 제목/요약/키워드: Label Standardization

검색결과 12건 처리시간 0.027초

스포츠 의류 라벨의 표준화 디자인 제안 -시각 정보디자인을 중심으로- (A Proposal for Standardization of Label Design on the Sports apparel -based on the visual information design-)

  • 배정연;김승인
    • 한국융합학회논문지
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    • 제8권12호
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    • pp.243-248
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    • 2017
  • 본 연구는 국외 스포츠의류의 라벨 표준화를 목표로 설정하였다. 라벨의 이론적 고찰을 통해 스포츠의류브랜드의 국외 상의 티셔츠를 중심으로 라벨을 조사하였다. 이를 토대로 32개 라벨 시안을 디자인하여 32명의 남녀 20~30대를 설문 조사하였다. 그 결과 피실험자는 size, fit, washing symbol mark, function의 정보표기를 선호하였다. 이와 같은 결과를 토대로 균형성, 간결성, 위계성, 인지성, 조화성을 고려한 보완된 라벨을 디자인하였다. 연구대상은 20~30대 남녀 12명을 심층 인터뷰하였다. 그 결과 피실험자는 자간과 공간, 정보표기 강조의 최대, 최소화로 인하여 라벨의 인지 선호도를 선정한다는 것을 알 수 있었다. 본 연구의 결과를 토대로 라벨 표준화를 활용하면 의류의 필수 정보를 쉽고 빠르게 인지할 수 있고, 소비자와 브랜드의 원활한 소통이 이루어질 것으로 판단한다. 또한, 언어의 통일화와 표준화된 라벨을 통해 소비자들은 얻고자 하는 정보를 쉽게 식별할 것으로 기대한다.

ATM 망에서의 레이블 스위칭 기법 성능 평가 및 분석 (Performance Evaluation of Label Switching in ATM networks.)

  • 이수경;오경희;손홍세;송주석
    • 한국통신학회논문지
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    • 제25권3B호
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    • pp.437-445
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    • 2000
  • 인터넷의 등장과 네트워킹 기술의 빠른 발전은 다양한 응용의 등장 및 사용자의 증가에 의한 대역폭 요구 증가 등의 변화를 가져왔다. 이러한 변화와 기존 라우터의 한계점으로 인해 스위칭과 라우팅 장비의 고성능화, 확장된 라우팅 기능 제공 등이 필요하게 되었고, 이를 위하여 IETF는 현재 MPLS라는 레이블 스위칭(Label Switching)방식을 표준화 중이다. 본 논문에서는 이 기술에 대한 성능을 분석하였다. 표준 및 스위치 개발이 연구 중인 현시점에서, 레이블 스위칭 기술의 성능 평가 결괴는 특히, ATM의 스위청 능력과 IP 계층 능력의 효율적인 활용의 기반 자료가 될 것이다. 본 논문은 라우터와 레이블 스위치를 포함하는 망을 구성하고 NLANR에서 제공하는 인터넷 트래픽을 입력 트래픽 소스로 하여 성능 평가를 수행하였으며, 레이블 스위칭의 구조 및 ATM testbed에서의 구현시, 이 기술이 갖는 스위칭의 기능성 및 성능을 분석하였다.

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수산나프로닐 캡슐 및 염산트라마돌 캡슐의 용출시험에 관한 연구 (Development of the Dissolution Tests for Nafronyl Oxalate Capsules and Tramadol Hydrochloride Capsules)

  • 황정분;문현주;고서연;장기욱;이규하;손경희;김인규;조대현
    • 약학회지
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    • 제55권5호
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    • pp.411-418
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    • 2011
  • The dissolution test method and an analytical procedure by HPLC were developed and validated for nafronyl oxalate capsules and tramadol hydrochloride capsules. These drugs were not yet characterized by the dissolution specifications in the Korean Pharmaceutical Codex. So, with each reference and test drugs, we did the preliminary and standard experiments based on the Korean Pharmacopeia Guideline of dissolution testing for solid oral dosage forms. The dissolution test for nafronyl oxalate capsules was carried out under sink conditions as follows: dissolution medium phosphate buffer pH 6.8, paddle rotation speed 100 rpm and vessel volume 900 ml. More than 80% of its label amount was released within 30 min in this method. Also the dissolution test for tramadol hydrochloride capsules was carried out under sink conditions as follows: dissolution medium water, paddle rotation speed 50 rpm and vessel volume 900 ml. More than 90% of its label amount was released within 15 min in this method. The dissolution samples were analyzed with a validated HPLC analytical procedure. The analytical methodology showed acceptable values in terms of specificity, linearity, precision and accuracy. The dissolution test methods described above were adequate for the purpose and may be proposed as a pharmacopeial standard to assess the performance of nafronyl oxalate capsules and tramadol hydrochloride capsules. Furthermore, the outcomes of this study were expected to help create an environment where safe and high quality drugs would be distributed on the domestic market making contributions to advancing public health.

국내외 바이오 플라스틱 표준화 및 식별표시 제도 동향 (Bio Plastics standardization and Eco Label System Trend in Domestic and Foreign Country)

  • 유영선
    • 월간포장계
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    • 통권251호
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    • pp.51-63
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    • 2014
  • 바이오 플라스틱, 에코패키징, 인체 무해성 등과 관련하여 국내외적으로 다양한 규격 및 시험방법이 있다. 바이오 플라스틱(Bio plastics)은 최근 생분해 플라스틱(Biodegradable plastics), 산화생분해 플라스틱(Oxo biodegradable plastics), 바이오 베이스 플라스틱(Bio based plastics)의 3가지로 나뉘어지고 있는 추세이다. 생분해 플라스틱 규격기준은 국제규격인 ISO 14855를 기준으로 국가별로 자국내 규격기준이 제정되어 있고, 이에 따른 인증마크를 시행하고 있다. 최근에 아랍에미레이트(UAE)에서 국제 환경규제를 전면 시행하면서 부각되고 있는 산화생분해 플라스틱은 미국의 ASTM D 6954:2004, ISO 14855 등의 기준을 토대로 제정한 UAE S 5009:2009에 의해 시행되고 있다. 또한 산업화가 급속하게 추진되고 있는 바이오 베이스 플라스틱 관련한 규격 기준은 미국 ASTM D 6866을 기준으로 시행되고 있고, 일부 국가는 자국내 규격기준을 제정하여 인증라벨을 부여하고 있다. 현재 바이오 베이스 플라스틱 인증라벨은 2002년 미국을 시작으로 2006년 일본, 2009년 벨기에, 2010년 독일, 2011년 한국에서 시행되고 있다. 그 외에도 GR마크, 녹색 인증, 단체 규격 인증, 업계 자체 규격 기준 등이 다양하게 시행되고 있다.

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친환경 농산물의 인증제도 및 정책에 대한 소비자 인지도 조사연구 (Consurmer's Recognition for the Label System and Policy of Environment-Friendly Agricultural Products)

  • 신철노;김진석
    • 농업생명과학연구
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    • 제43권3호
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    • pp.63-75
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    • 2009
  • 본 연구에서는 소비자 지향적 마케팅시대에 직면하여 국내외 농산물 소비수요의 변화에 대응하고 친환경농산물의 유통개선을 도모하기 위하여 소비자들의 친환경농산물인증제도 및 정책에 대한 인식을 조사분석 하였다. 조사연구 결과에 의하면 첫째, 친환경농산물의 소비저변을 확대시키기 위한 가장 시급한 문제는 생산자인 농민들이 아니라 소비자들에 대한 신뢰성을 확보하는 것이 무엇보다도 중요함을 알 수 있다. 이를 위해서는 다양하고 안전한 판로개척과 품질경쟁력 제고, 소포장 규격화 판매, 품질인증제도를 통한 브랜드화 추진, 리콜제 실시등을 통해 소비자들로부터 신뢰를 얻어야 한다. 둘째, 정부의 친환경농산물정책에 대한 지속적이 홍보와 교육이 이루어지고 또한 감독강화가 이루어져야 할 것으로 생각된다. 특히 친환경농산물 유통구조에서 농민들과 직접 거래를 하는 직거래나 인터넷 거래를 활성화시킴으로서 소비자들에 의한 신뢰도를 높일 수 있는 계기가 마련될 것이다. 셋째, 친환경농산물에 대한 품질관리가 지속적으로 이루어져야 한다. 이는 중앙정부의 감독관리도 중요하지만 지역별 품질인증기관을 육성하고 품질인증기관이 생산과정에 대한 투명성을 철저히 보장할 수 있도록 제도화하여 친환경농산물에 대해 소비자들로부터 신뢰를 얻어야 할 것으로 보인다. 마지막으로 친환경농산물 생산농가가 판매에 대한 어려움을 지자체 등이 적극적으로 지원할 필요가 있을 것으로 판단된다.

희소금속 재활용을 위한 ITU-T 국제표준 개발현황 (Status of ITU-T International Standard Development on Rare Metal Recycling)

  • 이미혜;최원정;서석준;김범성
    • 한국분말재료학회지
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    • 제23권4호
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    • pp.325-330
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    • 2016
  • Owing to increasing demand of rare metals present in ICT products, it is necessary to promote the rare metal recycling industry from an environmental viewpoint and to prevent climate change. Despite the fact that information for toxic substances is partly indicated, a legal basis and an international standard indicating usage of rare metals is insufficient. In order to address this issue, a newly created study group of environment and climate change at the ITU (International Telecommunication Union) is doing research to develop methodologies for recycling rare metals from ICT products in an eco-friendly way. Under this group, the Republic of Korea has established two international standards related to rare metals present in ICT products. The first is 'Release of rare metal information for ICT products (ITU-T L.1100)' and the other is 'Quantitative and qualitative analysis methods for rare metals (ITU-T L.1101)'. A new proposal for recommending the provision of rare metal information through a label by manufacturers and consumer/recycling businesses has been approved recently and is supposed to be published later in 2016. Moreover, these recommendations are also being extended to IEC, ISO and other standardization organizations and a strategy to reinforce the ability for domestic standardization is being established in accordance with industrial requirements. This will promote efficient recycling of rare metals from ICT products and will help improve the domestic supply of rare metals.

Unsupervised Outpatients Clustering: A Case Study in Avissawella Base Hospital, Sri Lanka

  • Hoang, Huu-Trung;Pham, Quoc-Viet;Kim, Jung Eon;Kim, Hoon;Park, Junseok;Hwang, Won-Joo
    • 한국멀티미디어학회논문지
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    • 제22권4호
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    • pp.480-490
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    • 2019
  • Nowadays, Electronic Medical Record (EMR) has just implemented at few hospitals for Outpatient Department (OPD). OPD is the diversified data, it includes demographic and diseases of patient, so it need to be clustered in order to explore the hidden rules and the relationship of data types of patient's information. In this paper, we propose a novel approach for unsupervised clustering of patient's demographic and diseases in OPD. Firstly, we collect data from a hospital at OPD. Then, we preprocess and transform data by using powerful techniques such as standardization, label encoder, and categorical encoder. After obtaining transformed data, we use some strong experiments, techniques, and evaluation to select the best number of clusters and best clustering algorithm. In addition, we use some tests and measurements to analyze and evaluate cluster tendency, models, and algorithms. Finally, we obtain the results to analyze and discover new knowledge, meanings, and rules. Clusters that are found out in this research provide knowledge to medical managers and doctors. From these information, they can improve the patient management methods, patient arrangement methods, and doctor's ability. In addition, it is a reference for medical data scientist to mine OPD dataset.

일본과 한국의 기능성 유제품의 규격기준 및 시장현황에 관한 연구 (Investigation of Legal Regulation and Market Circumstances for Functional Dairy Products in Korea and Japan)

  • 박다정;이단원;박정민;신진호;김지연;전상록;송태석;윤성식;김진만
    • 한국축산식품학회지
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    • 제29권4호
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    • pp.523-532
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    • 2009
  • Changing health awareness has had an important effect on the functional food industry and is creating greater market opportunities. Unfortunately, there is no statement on functional dairy products in the Processing of Livestock Products Act. As a result, there is confusion in the market and legal difficulties with regard to the advertising of functional dairy products. This study was carried out to improve the current standardization of functional dairy products by comparing the domestic Health/Functional Food Act with the Japanese Health Promotion Law, and by investigating scientific data and articles from various literature and the Internet. In Japan, the Ministry of Health, Labor, and Welfare (MHLW) officially presented the Food with Health Claims (FHC) system that consists of Food with Nutrient Function Claims (FNFC), and innovated Food for Specified Health Uses (FOSHU). In 2005, the FOSHU system was changed to include several new subsystems: Current, Standardized, Reduction of disease risk, and Qualified FOSHU. Finally, to manufacture FOSHU, scientific evidence pertaining to such products must be examined by MHLW. Since FNFC was allowed, only 12 vitamins, ${\beta}-carotene$, and five minerals were approved, though without scientific evidence of efficacy. The Korean Health/Functional Food Act requires that health/functional foods (HFFs) be marketed in measured doses. There are two types of HFFs: generic and product-specific. There are 67 ingredients listed in the act for generic HFFs, and if an HFF has a new active ingredient, it is considered a product-specific HFF. Product-specific HFFs must be approved by the Korean Food and Drug Administration (KFDA). With the present standards, it is impossible to label and advertise functional dairy products with health/functional claims. Government agencies must cooperate to solve this problem, and standardization should be carried out by considering existing health/functional products and claims/indications from other countries.

고시 수재 의약품 중 피라세탐 정 및 브롬화수소산페노테롤 정의 용출시험법 개발 (Development of Dissolution Testing Method for Piracetam Tablets and Fenoterol Hydrobromide Tablets in Korean Pharmaceutical Codex)

  • 김은정;이진하;박찬호;손경희;김인규;김동섭;사홍기;최후균
    • 약학회지
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    • 제55권4호
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    • pp.324-331
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    • 2011
  • Although the dissolution test can serve as an effective tool for quality control and predictor of in vivo performance, there are a number of drugs with no established dissolution specifications in Korean Pharmaceutical Codex (KPC). Among those commercially available, Piracetam Tablets and Fenoterol hydrobromide Tablets were selected to develop the dissolution testing method. The dissolution condition was determined based on the "Guidelines on Specifications of Dissolution tests for Oral dosage forms" of Korea Food & Drug Administration (KFDA). The dissolution test for Piracetam Tablets was carried out under sink condition with distilled water as dissolution medium, paddle rotation speed at 50 rpm and medium volume of 900 ml. More than 80% of its label claim was released within 30 min. In case of Fenoterol hydrobromide Tablets, distilled water was also found to be suitable to ensure sink condition. The rotation speed of 50 rpm and 900 ml of dissolution medium were used to evaluate the dissolution profile. The dissolution rate of fenoterol hydrobromide was over 90% in 15 min. The HPLC analysis methods were validated in terms of accuracy, precision, specificity, linearity, quantitation limit and range. The results suggested that the analytical methods used are simple and suitable to measure the dissolution rate of piracetam and fenoterol hydrobromide. Therefore, the analysis methods could be utilized in setting dissolution specifications of Piracetam Tablets and Fenoterol hydrobromide Tablets in the revised version of KPC.

20대 소비자의 탁주 이용실태 및 만족도 조사 (Consumption and Satisfaction Evaluation of Takju among Consumers Ages 20 to 29)

  • 정은경;김수정;주나미
    • 대한영양사협회학술지
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    • 제17권1호
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    • pp.47-57
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    • 2011
  • The purpose of this research was to investigate consumption and satisfaction of Takju (Makgeolli) among consumers ages 20 to 29 living in Seoul and Gyeonggi province. It was found that 86.2% of the respondents drank Takju once or twice a month, and the high satisfaction group drank Takju with a frequency of 8 times a month (P<0.01). Respondents selected market (44.4%) and restaurants (34.9%) as the most common place of purchase, whereas pub (42.2%) and Takju bar (32.8%) were the drinking places selected. Regarding the preferred ingredients, respondents liked pear the most followed by Lycium chinense, corn, pine nuts, ginseng, and citrus fruit. The most compatible foods with Takju were identified as Buchimgae (Jeon) (97.4%), Kimchi (45.6%), Bokkeum (36.4%), Namul & Muchim (25.0%), and Jjim (21.5%). Pajeon was mentioned as the most compatible food with Takju, followed by Bulgogi, Gamjatang, Agwijjim, Dubukimchibokkeum, and Ojingeotwigim. Regarding consumers' satisfaction of Takju, taste was the most highly valued, with color, price, alcohol content, function, flavor, diversity of raw materials, and accuracy of label also highly considered. Further, to formulate a plan to encourage consumption of Takju, the high satisfaction group decided that promotion of local festivals and events related to Takju, standardization of quality, creation of brands, expansion of distribution network, and organization of relevant departments are the most important compared to other items (P<0.05).