게시판-관련소식
뉴스레터 2015년 8월호
2015-09-09 by ISPE Korea
ISPEAK 2015년 8월호
◇◇ GMP소식 ◇◇
의약품 소량포장단위 공급에 관한 규정」개정고시안 행정예고 알림 병포장의 소량포장 공급단위를 30정․캡슐 ‘이하’로 개선하고 공급제형에 시럽제(건조시럽제 제외)를 추가하는 한편, 차등적용 비율 탄력적 확대 근거 및 당해연도 처음 허가 또는 신고되어 공급된 의약품의 소량포장 공급 예외 근거를 마련하는 등 의약품 소량포장단위 공급 제도를 개선하려는 것임. Continue Reading
Warning Letters 2015 These letters are supplied by the CDER Freedom of Electronic Information Office. This page only covers Office of Prescription Drug Promotion (formerly Division of Drug Marketing, Advertising and Communications) and CDER Headquarters Warning Letters.
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◇◇ 가이드라인소식 ◇◇
Request for Quality Metrics, Guidance for Industry Quality metrics are used throughout the pharmaceutical industry to monitor quality control 16 systems and processes and drive continuous improvement efforts in drug manufacturing. These 17 metrics can also be used by FDA: to help develop compliance and inspection policies and 18 practices, such as risk-based inspection scheduling of drug manufacturers; to improve the 19 Agency’s ability to predict, and therefore, possibly mitigate, future drug shortages; and to 20 encourage the pharmaceutical industry to implement state-of-the-art, innovative quality 21 management systems for pharmaceutical manufacturing. ---------------------------------------------------------------------------------------------
◇◇ ISPE 국내외소식 ◇◇ PHARMACEUTICAL ENGINEERING 한글번역 예정 Jul/ Aug 2015 Volume 35, Number 4 -INNOVATIVE MANUFACTURING PROMOTES QUALITY -SCIENTIFIC AND REGULATORY CONSIDERATIONS FOR IMPLEMENTING MATHEMATICAL MODELS IN THE QUALITY BY DISIGN FRAMEWORK -SINGLE-USE FREEZE-THAW SYSTEMS: A PROCESS IN TRANSITION FOR THE PHARMACEUTICAL INDUSTRY -AN ELECTRONIC FORMAT FOR DATA EXCHANGE BETWEEN RAW MATERIAL SUPPLIERS AND END USERS ENABLES SUPERIOR KNOWLEDGE MANAGEMENT -TESTS ON ROUGING AND EXPERIENCES DEALING WITH ROUGING IN PHARMACEUTICAL PRODUCTION
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