게시판-관련소식
뉴스레터 2015년 2월호
2015-02-25 by ISPE Korea
ISPEAK 2015년 2월호
◇◇ GMP소식 ◇◇ 원료의약품 제조 및 품질관리기준(GMP) 가이던스 `15.7.1일자로 신설된 원료의약품 GMP 기준이 적용됨에 따라, 식품의약품안전처에서는 원료의약품 제조업체의 GMP에 대한 이해도와 실제 적용의 유연성 제고를 위한 원료의약품 GMP 가이던스를 붙임과 같이 마련해 발간합니다. Continue Reading
의약품 제조 및 품질관리에 관한 규정 행정예고 식품의약품안전처 공고 제2015 - 35호
Guidance Agenda : New & Revised Draft Guidances CDER is Planning to Publish During Calendar Year 2015 (PDF - 46KB) ---------------------------------------------------------------------------------------------
◇◇ 가이드라인소식 ◇◇
PET Drugs — Current Good Manufacturing Practice (CGMP) This guidance represents the Food and Drug Administration’s (FDA’s) current thinking on this topic. It does not create or confer any rights for or on any person and does not operate to bind FDA or the public. You can use an alternative approach if the approach satisfies the requirements of the applicable statutes and regulations. If you want to discuss an alternative approach, contact the FDA staff responsible for implementing this guidance. If you cannot identify the appropriate FDA staff, call the appropriate number listed on the title page of this guidance.
Electromagnetic Compatibility Aspects of Medical Device Quality Systems This guide was prepared by the FDA, Office of Regulatory Affairs, and the Center for Devices and Radiological Health (CDRH), Office of Compliance. This guide provides FDA investigators with information regarding electromagnetic compatibility (EMC) and how it is likely to be addressed in a medical device firm's Quality System/Good Manufacturing Practices (QS/GMP) (21 CFR Part 820). Terms throughout this document that are in bold typefacex are defined in Appendix A.
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◇◇ ISPE 국내외소식 ◇◇ PHARMACEUTICAL ENGINEERING 한글번역 (JANUARY/FEBRUARY 2014 Volume 35, Number 1)
- Risk Assssment : Issues and Chalenges - Science - Based Quality Risk Management - Risk Analysis and Annual Training Program Definition - Implementation of QbD using MES - ISPE update 유료회원에게 무료로 배포하고 있습니다
2015 ISPE KOREA 정기교육 안내 ISPE KOREA 상반기 정기교육 FDA'S System-based GMP Inspections Good Laboratory Practice (GLP) FDA's GLP Inspection Biosafety Regulations CGMP vs. Biosafety in designing CGMP Facilities - 일시 : 2015.04.29(수) 09:30~16:30 - 강사 : 이정길 (WHO, KFDA) - 장소 : 차세대융합기술연구원 세미나실
ISPE KOREA 하반기 정기교육 The Latest CGMP trends for Drugs & Biologics : Risk-Based & Quality System Approach focusing on Enhanced Process/Product Understanding (ICH Q8-Q11) - Overview on the New Paradigm on CGMP for 21st Century - Hazard & Risk Analysis in Pharmaceutical Products (Application of HACCP methodology) - Quality System Approach to Pharmaceutical CGMP - Process Analytical Technology (PAT) - Sterile Drug Products Produced by Aseptic Processing - CGMP - 일시 : 2015.09.16(수) 09:30~16:30 - 강사 : 이정길 (WHO, KFDA) - 장소 : 차세대융합기술연구원 세미나실 자세한 사항은 www.ispe.or.kr 에서 확인하실 수 있습니다.
Upcoming Global Event
2015 Aseptic Annual Conference
2015 Statistics in PV Forum
2015 Quality Metrics Summit
2015 ISPE Europe Annual Conference
2015 ISPE/PQRI Quality Manufacturing Conference
2015 Pharma EXPO
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◇◇ 연간 회원 및 스폰서 안내 ◇◇ ♣ 회원가입 안내
♣ 스폰서안내 (단위 : 천원)
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