Gary Jeng：生物制药洁净厂房的设计

作者：本网编辑文章来源：PHT《制药业》发布时间：2017-06-12

Gary Jeng，美国西图建筑工程（上海）有限公司首席工艺建筑设计经理...

Gary Jeng，美国西图建筑工程（上海）有限公司首席工艺建筑设计经理

Gary Jeng

美国西图建筑工程(上海)有限公司首席工艺建筑设计经理

郑先生拥有超过25年的制药、生物制药、生物技术、实验室、工业/制造业和食品加工的工作经验。他在FDA和欧盟监管、NIH/ BSL生物监管、IBC建筑规范、ADA监管以及危险设施设计(NFPA，OSHA和FM的合规性)的cGMP和ISO(洁净室)验证方面具有丰富的知识和经验，以符合建筑审美和建筑功能的合规标准。

Mr. Jeng bring over 25 years of architectural experience to projects he has supported in the pharmaceutical, biotechnology, laboratory, industrial/manufacturing, food processing, corporate, institution, commercial, sports, recreation, multi-family, and residential facilities. He has knowledge and experience in cGMP and ISO (clean room) per FDA and EU’s regulatory, NIH/BSL biological regulatory, IBC building code, ADA regulatory, hazardous facility design (NFPA, OSHA and FM compliance), facility rationalization and coordination of design efforts to validate architectural aesthetic/functional compliance criteria is met.

Facility Type Design Experience

· Life Science industry – Laboratory, Pilot plan and Manufacturing facilities

· Biopharmaceutical and Biotech Process Architectural knowledge

· Pharmaceutical Facility Architectural knowledge

· Sterile & Aseptic Facility Architectural knowledge

Laboratory – BSL, Q/A, Q/C, R&D, Production Development laboratories

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Gary Jeng：生物制药洁净厂房的设计

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消防与洁净的矛盾，在洁净室围护结构中应该如何调节？

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