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嘉賓信息
發(fā)布時(shí)間: 2023 - 06 - 25
點(diǎn)擊次數(shù): 0
所屬職位: 副總裁兼首席運(yùn)營官
所屬公司: 貝達(dá)藥業(yè)股份有限公司
個(gè)人簡介:
香港科技大學(xué)高級(jí)管理人員工商管理碩士。曾就職于北京同仁醫(yī)院骨科,在美國百時(shí)美施貴寶、法國賽諾菲安萬特、美國禮來、英國阿斯利康、美國默沙東等醫(yī)療機(jī)構(gòu)和知名藥企擔(dān)任高層管理職務(wù),具有近30年的藥物推廣渠道建設(shè)和藥物可及性提升經(jīng)驗(yàn),特別是對(duì)腫瘤治療領(lǐng)域的藥物在中國市場的應(yīng)用具有專業(yè)影響力。分管公司腫瘤事業(yè)部、市場部、商務(wù)及市場準(zhǔn)入部。
發(fā)布時(shí)間: 2023 - 06 - 26
點(diǎn)擊次數(shù): 0
所屬職位: 首席科學(xué)家
所屬公司: 華潤醫(yī)藥
個(gè)人簡介:
陳波博士是海外高層次人才特聘專家, 目前擔(dān)任華潤醫(yī)藥集團(tuán)首席科學(xué)家, 在生物技術(shù)和制藥行業(yè)擁有超過20年的國際職業(yè)生涯,包括在美國NIH,AstraZeneca等頂尖科研機(jī)構(gòu)和制藥公司從事基礎(chǔ)研究和新藥研發(fā)團(tuán)隊(duì)領(lǐng)導(dǎo)者的工作經(jīng)歷,具有從靶點(diǎn)發(fā)現(xiàn)到臨床開發(fā)和商業(yè)運(yùn)作的整個(gè)研發(fā)價(jià)值鏈的研發(fā)背景。他博士畢業(yè)于中國人民解放軍空軍軍醫(yī)大學(xué),在美國NIH完成博士后,其后還獲得美國Hood College工商管理碩士學(xué)位。他迄今在著名期刊上發(fā)表國際學(xué)術(shù)論文,專著章節(jié)和專利共30余篇,包括發(fā)表在Annals of the Rheumatic Diseases, Nature  Communication, Nature Immunology, Nature Medicine, PNAS  等頂尖雜志上的論文。并曾獲得了衛(wèi)生部的科技進(jìn)步二等獎(jiǎng),AstraZeneca的員工白金獎(jiǎng)和銀獎(jiǎng),NIH的卓越研究員獎(jiǎng),齊魯制藥集團(tuán)的卓越領(lǐng)導(dǎo)獎(jiǎng)等。Dr. Bo Chen is a specially-appointed expert for overseas high-level talents . He is currently the Chief Scientific Officer at China Resources Pharmaceutical Group Limited.  He has more than 20 years of international career in the biotechnology and pharmaceutical industries, including basic research and innovative drug R&D team leadership in top scientific research institutions and pharmaceutical companies such as the National Institutes of Health, AstraZeneca, etc. He has R&D background in the entire R&D value chain from target discovery to clinical development and commercial operation. He received his PhD. degree from the Air Force Medical University (China), completed the postdoctoral fellowship at the National Institutes of Health in the United States, and later obtained an MBA degree from Hood College (U.S.A). He has published dozens of academic papers, book chapters  and patents in peer-reviewed journals, including papers published in top journals such as Annals of the Rheumatic Diseases, Nature Communication, Nature Immunology, Nature Medicine, PNAS, etc. And has won the second prize of the Ministry of Health's Science and Technology Progress Award, the AstraZeneca Staff Platinum Award and Silver Award, the NIH Outstanding Researcher Award, Qilu Pharmaceutical Group's Outstanding Leadership Award, etc.
發(fā)布時(shí)間: 2023 - 06 - 25
點(diǎn)擊次數(shù): 0
所屬職位: 高級(jí)副總裁
所屬公司: 綠葉制藥集團(tuán)
個(gè)人簡介:
孫志剛博士現(xiàn)任綠葉制藥集團(tuán)高級(jí)副總裁,負(fù)責(zé)整個(gè)集團(tuán)的國際研發(fā)、全球質(zhì)量、和全球藥物警戒等方面的工作。 他也曾在美國擔(dān)任太陽藥業(yè)有限公司監(jiān)管事務(wù)副總裁,負(fù)責(zé)新藥和仿制藥的上市注冊(cè)申報(bào)及上市后變更管理工作。 加入工業(yè)界之前,孫博士曾在美國FDA工作近12年,擔(dān)任工藝設(shè)施辦公室(OPF)工藝評(píng)審II處代理主任,主要負(fù)責(zé)新藥和仿制藥的質(zhì)量審評(píng)和批準(zhǔn)前檢查(PAI)。他還擔(dān)任過FDA仿制藥辦公室(OGD)CMC審評(píng)組組長以及FDA駐華辦公室(北京)代理藥品助理主任。除藥物質(zhì)量審評(píng)和GMP現(xiàn)場檢查外,孫博士也應(yīng)邀加入多個(gè)FDA技術(shù)委員會(huì),參與制定藥物審評(píng)的內(nèi)部政策程序及外部企業(yè)指南, 并多次獲得FDA獎(jiǎng)勵(lì)。目前他應(yīng)邀擔(dān)任2020-2025界美國藥典委員會(huì)委員(USP Expert Committee)和專家組(USP Expert Panel)成員, 以及中國醫(yī)藥創(chuàng)新促進(jìn)會(huì)國際創(chuàng)新藥物監(jiān)管專業(yè)委員會(huì)委員。Dr. Zhigang Sun is currently Senior Vice President at Luye Pharma Group Ltd.,responsible for international R&D, global quality, and global pharmacovigilance. He previously served as Vice President of Regulatory Affairs at Sun Pharmaceutical Industries, Inc. in the United States, where he was responsible for the marketing registration and post-market change management of new drugs and generic drugs. Prior to joining industry, Dr. Sun worked at U.S. FDA for nearly 12 years, where he served as the acting Branch Chief at Office of Process and Facilities (OPF), and was responsible for  quality review and pre-approval inspection (PAI) of new drugs and generic drugs. He also served as the CMC team Leader at Office of Generic Drugs (OGD), FDA, and the acting Assistant Country Director for Drugs at FDA China Office (Beijing).  In addition to drug review and CGMP inspection, Dr. Sun involved in developing CDER Manual of Policies and Procedures (MaPP) and FDA Guidance for Industry in several FDA technique committees, and has been awarded many times within the FDA owing to his excellent contribution.  He is currently invited to serve as a member of the USP Expert Committee and a member of the USP Expert Panel in 2020-2025, as well as a member of the International Innovative Drug Regulatory Committee of the China Association for the Promotion of Pharmaceutical Innovation.
發(fā)布時(shí)間: 2023 - 06 - 25
點(diǎn)擊次數(shù): 0
所屬職位: 研發(fā)總經(jīng)理
所屬公司: 濟(jì)民可信集團(tuán)上海濟(jì)煜醫(yī)藥科技有限公司
個(gè)人簡介:
崔海峰 濟(jì)民可信集團(tuán)副總裁,研發(fā)中心首席科學(xué)家兼總經(jīng)理。崔海峰畢業(yè)于浙江大學(xué)高分子化學(xué)專業(yè),后參加工作任助理工程師,在浙江省化工研究院從事高分子材料研發(fā)工作,期間一成果獲國家科學(xué)進(jìn)步二等獎(jiǎng)。 1997年進(jìn)入美國賓西法尼亞大學(xué)深造,于2002年獲有機(jī)化學(xué)博士。2002年起加入位于美國費(fèi)城都會(huì)區(qū)的英國大型制藥公司GSK從事原創(chuàng)新藥研發(fā),歷任資深科學(xué)家,研究員,主任科學(xué)家至科學(xué)總監(jiān),先后領(lǐng)導(dǎo)過十余個(gè)新藥項(xiàng)目,覆蓋靶點(diǎn)發(fā)現(xiàn)到臨床PoC全流程,目前有四個(gè)項(xiàng)目進(jìn)入臨床,其中一個(gè)進(jìn)入臨床三期。 主要疾病領(lǐng)域在心血管,傳染病,免疫及腫瘤。2019年10月回到中國,加入J&J亞太創(chuàng)新中心任資深總監(jiān),負(fù)責(zé)在亞太地區(qū)打造新藥研發(fā)的生態(tài)圈,以及尋求與當(dāng)?shù)貏?chuàng)新公司和科研院所的合作機(jī)會(huì),疾病領(lǐng)域包括傳染病及疫苗,神經(jīng)科學(xué),心血管及代謝,和免疫。2021年3月加入濟(jì)民可信,負(fù)責(zé)整體的研發(fā)工作。Haifeng Cui: Chief Scientific Officer,  Head of R&D, Jemincare Group; SAPA-China Executive CouncilPhD in organic chemistry from University of Pennsylvania. Started his drug discovery career at GSK from 2002 in the USA, worked across several therapeutic areas including cardiovascular, renal disease and infectious disease, over the years led multi-discipline teams delivered several compounds into clinic and follow-up to human PoC. From 2019, he returned to China and jointed J&J, performing search and evaluation for opportunities up to phase 2a to feed into global pipeline, covering infectious disease & vaccine, immunology, neuroscience, cardiovascular & metabolic diseases in the APAC region. Currently he leads the R&D organization of Jemincare Group, advancing an extensive portfolio of innovative medicines into clinical practice.
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