본 연구에서는 어린이 기호식품 중 하나인 과자류(과자, 캔디류, 츄잉껌, 빙과류)에 대하여 1,005건(과자 250건, 캔디류 255건, 츄잉껌 250 건, 빙과류 250건)에 대해 위생 지표 미생물인 일반세균 수, 대장균군/대장균과 더불어 식중독 원인균인 바실러스 세레우스, 클로스트리디움 퍼프 린젠스 및 황색포도상구균에 대한 미생물 검사를 실시하였다. 과자류에 대한 일반세균 수의 경우 전체 시료의 26.8%에서 검출되었고, 검출된 세균 수는 1.7 log CFU/g을 나타내었다. 유형별로 살펴보았을 때에는 과자 250건 중 45.2%의 시료에서 검출되었으며, 빙과류 28.8%, 캔디류 20.0% 및 츄잉껌 13.2% 순으로 검출되는 것으로 확인되었다. 다른 위생지표 세균인 대장균군/대장균의 경우는 모든 시료에서 검출되지 않았다. 식중독균을 분석한 결과에서는 캔디류를 제외한 나머지 유형에서 바실러스 세레우스만 검출이 되었고, 평균 검출량은 1.4~1.6 log CFU/g로 현행 식품공전상의 미생물규격인 3 log CFU/g 이하 수준으로 모두 적합한 제품이었다. 이는 식품공전 상에서 정 하고 있는 미생물 규격에 비해서는 낮은 수치로 식품의 제조·유통에는 문제가 없는 것으로 보이지만, 식중독 민감도가 높은 어린이들에게 안전한 식품을 제공하기 위해 합리적이고 과학적인 미생물 기준규격을 고려해야 한다.

It is well understood that developing new drugs is one of the highest value-added businesses in a country; however, the current governments' spending in pharmaceutical research and development(R&D) is minimal in Korea. This paper suggests that different governmental bodies should take in charge of different stages of the R&D process in order to maximize the use of limited government research funding. First, during the initial phase of the drug development, including clinical trials, the Ministry of Education, Science and Technology is the most appropriate governmental organization to support the research. For later procedures such as supporting the industries for exporting developed drugs, legislative approvals, and building infrastructure for future clinical trials should be supported by the Ministry of Knowledge and Economy and the Ministry of Health and Welfare along with the Korea Food and Drug Administration(KFDA). The KFDA, which is the main governmental agency approving newly developed drugs in the market, will need to take a crucial responsibility in the initial phase of the pharmaceutical R&D by guiding the industries with timely and proper information. As a first step, it is recommended to set up and operate a center for supporting new drugs, so that the industries can facilitate the development of marketable drugs which meet customers' needs. Later, in order to expedite the process of exporting and getting approvals of the newly developed drugs from foreign countries, it is necessary to develop new approval system, which includes introduction of the Good Manufacturing Practice (GMP), mandatory validation system, and education program for supporting expertise. Lastly, the KFDA needs to take an active role in developing Korean pharmaceutical industries by communicating with other foreign governments with regards to the globalization of the Korean pharmaceutical industries. For example, as a follow up after the Free Trade Agreement(FTA), active discussion on GLP of Mutual Recognition Agreement(MRA) with the United States of America, should be seriously considered.

As Standards and Specifications of the Saengsik-classes has been established since 2005 by KFDA. The microbial Standards and Specifications of the Saengsik-classes is as follows; no detection in Escherichia coli, colony forming unit less then 1,000/g in Bacillus cereus, colony forming unit less then 100/g in Clostridium perfringens respectively. Contamination levels of Total aerobic bacteria, Escherichia coli,, Bacillus cereus and Clostridium perfringens in Saengsik-classes were monitored. Total aerobic bacteria counts in Saengsik-classes was 1×10¹~5.3×107 cfu/g, for Bacillus cereus 1×10²~9×10² cfu/g, for Clostridium perfringens 1×10¹ cfu/g. Escherichia coli, was not isolated from all Saengsik-classes. Thess results will provide information for introduction of HACCP system to ensure microbial safety of Saengsik-classes.

In this study, microbial investigation is accomplished for 554 Jeot-kal samples (102 of Jeot-kal, 448 of Seasoned Jeot-kal and 4 of Sik-khe, respectively) that corresponds with Coliform-bacteria, Escherichia coli, Aerobic live bacteria as hygienic indicator microorganisms, and Staphylococcus aureus, Vibrio parahaemolyticus as Food-borne pathogenic microorganisms. Based on the methods in Korea Food Code, reliable data are obtained as follows; in 31.9% rate of the samples, Coliform bacteria are verified in the extent of 0~20,000 CFU/g as 2.3 logCFU/g. Especially, Seasoned Jeot-kal (37.7%, 2.3 logCFU/g) are detected to 6 and 2 folds higher than those of Jeot-kal, 5.9% and 1.4 logCFU/g. Likewise, Escherichia coli is detected from 9 samples only in Seasoned Jeot-kal, that includes seasoned squid, seasoned octopus, seasoned roe of pollack, seasoned large-eyed herring and seasoned hairtail. Aerobic live bacteria are also detected in the range of 0~8.9 × 108 CFU/g. Against salinity, E. coli are detected in samples only less than 10% salinity. Concomitantly, aerobic live bacteria count is decreased to 5.5~3.6 log CFU/g upon the salinity is increased up to 25%. However, S. aureus and V. parahaemolyticus are not detected in 554 samples, presumptively referring Jeot-kal products are somehow free from such food-borne pathogens. As the results above, we deliberately consider that the sanitary control in Jeot-kal, which be necessarily fermented- as well as non-microbially inactivated should be ensured in near future and also suggest an effectual microbial standard corresponding to the Negativity in E. coli for Jeot-kal products.