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학술논문

한약ㆍ생약제제 품목허가신고심사 규정 변화에 관한 고찰

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영문명
A Study on the Changes in Regulations Regarding Approval, Notification and Review of Herbal Medicinal Preparations and Crude Drug Preparations -From 1948 to 2012-
발행기관
한국의사학회
저자명
엄석기(Seok Ki Eom)
간행물 정보
『한국의사학회지』제27권 제2호, 11~37쪽, 전체 27쪽
주제분류
의약학 > 한의학
파일형태
PDF
발행일자
2014.12.31
6,040

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국문 초록

영문 초록

Objectives : The purpose of this study was to analyze and identify the problems of the changes in regulations that are relevant to approval, notification, and review of herbal medicinal preparations and crude drug preparations. Methods : I collected the regulations of approval, notification, and review of medicinal products mostly from official gazettes, analyzed enactment and amendments regarding herbal medicinal preparations and crude drug preparations, and studied it from the view point of Korean medicine field. Results : Regulations in regards to approval, notification, and review of herbal medicinal preparations and crude drug preparations were first established in 1978. Herbal drugs started to be categorized as crude drug preparations in 1981 and the regulatory outlines were completed in 1999. From 2008 to 2012, the regulatory standards that let crude drug preparations be new drugs from natural products were established. Through those procedures, the followings became crude drug preparations: 1) wholly new prescriptions that are not recorded in Korean Medical Classics, 2) prescriptions that are recorded in Korean Medical classics but prepared with new standard, composition and efficacy, 3) prescriptions that are recorded in Korean Medical classics but prepared with new formulation, and 4) herbal drugs. In case of herbal medicinal preparations, however, only regulations that are related to 1) drugs prepared with new compositions that are not recorded in Korean Medical Classics, 2) drugs with same prescription and same formulation, and 3) drugs with new formulation were arranged. Conclusions : Actual circumstances on crude drug-oriented regulations regarding approval, notification and review and future forms of prescription and drug administration in Korean Medical Institutions can be expected due to expansion in range of herbal medicinal preparations and shrink in that of on-site preparations. Reasonable improvement in efficient usage of modernized herbal medicinal preparations in Korean medical institutions and prospective cooperation from related pharmaceutical industry are needed.

목차

Abstract
Ⅰ. 서론
Ⅱ. 연구 방법
Ⅲ. 본론
Ⅳ. 고찰
Ⅴ. 결론
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APA

엄석기(Seok Ki Eom). (2014).한약ㆍ생약제제 품목허가신고심사 규정 변화에 관한 고찰. 한국의사학회지, 27 (2), 11-37

MLA

엄석기(Seok Ki Eom). "한약ㆍ생약제제 품목허가신고심사 규정 변화에 관한 고찰." 한국의사학회지, 27.2(2014): 11-37

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