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세미나·강연
작성자 관리자 작성일 2017.09.15
제목 2017 글로벌 바이오의약품 인허가제도 실무교육 연자소개 조회수 52,854

John Geigert

Ph.D., RAC, President of

BioPharmaceutical Quality Solutions





John Geigert is President of BioPharmaceutical Quality Solutions, which for the last 15 years has specialized in providing CMC regulatory strategy consulting for the biopharmaceutical industry. He has over 40 years of CMC industrial experience and leadership in the biopharmaceutical industry.


He has held senior management positions as Vice President of Quality at both IDEC Pharmaceuticals Corporation in San Diego and Immunex Corporation in Seattle, and he was Director of Product Development at Cetus Corporation in Berkeley. At these companies, he helped lead the CMC efforts to obtain regulatory approvals for 6 biopharmaceutical products now commercially available in the U.S. and in Europe.


John Geigert has served on the PDA Board of Directors, currently chairs the PDA Biopharmaceutical Advisory Board, and has served as an expert member of the USP Biotechnology Committee. He is the author of the book The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2nd Edition, and has written extensively for RAPS Focus (What Senior Management Needs to Know About CMC Regulatory Compliance for Biotech Products (Aug-Nov 2009, 4-part series)), Demystifying CMC Regulatory Strategy (Sept 2011-Mar 2012, 4-part series).


John Geigert obtained his B.S. in Chemistry from Washington State University and his Ph.D. degree in Organic/Analytical Chemistry from Colorado State University.



John Geigert BioPharmaceutical Quality Solutions 대표는 바이오의약품 산업의 CMC 분야에서 40년 이상의 경력을 가지고 있다. BioPharmaceutical Quality Solutions는 지난 15년 동안 바이오의약품 CMC 인허가 전략에 대한 컨설팅을 진행했다.


그는 미국 제약회사인 IDECImmunex의 품질담당 부사장 및 Cetus사의 제품 개발 책임자를 역임했다. 이들 회사에서 그는 현재 미국과 유럽에서 판매되는 6개의 바이오의약품의 인허가 승인을 얻기 위한 CMC 기반을 구축하는데 일조했다.


John Geigert 대표는 최근 PDA(제약기술과 GMP를 다루는 국제 학술단체)의 바이오의약품 자문위원회 위원장과 USP (미국 약전) 바이오기술 위원회의 전문위원으로 활동하고 있다. 그는 ‘The Challenge of CMC Regulatory Compliance for Biopharmaceuticals and Other Biologics 2nd Edition’의 저자이며, RAPS Focus (What Senior Management Needs to Know About CMC Regulatory Compliance for Biotech Products (Aug-Nov 2009, 4-part series)), Demystifying CMC Regulatory Strategy(Sept 2011-Mar 2012, 4-part series)를 집필했다.


John Geigert 대표는 Washington State Universit에서 화학 학사학위를, Colorado State University에서 유기/분석화학 박사학위를 취득했다.



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이전글 2017 글로벌 바이오의약품 인허가제도 실무교육 일정
다음글 2017 글로벌 바이오의약품 인허가제도 실무교육 소개