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Tofflon Webinar – Innovative Vaccine Technology Transfer and Local Manufacturing

April 30, 2024
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April 30th, 2024

Time: 11 AM – 01 PM (CET)

Title: Tofflon Webinar – Innovative Vaccine Technology Transfer and Local Manufacturing

Description: After the COVID-19 epidemic, more and more pharma emerging markets and countries strongly demand localized manufacturing. “Innovative Vaccine Technology Transfer and Local Manufacturing” becomes one of the main streams of local industry growth. To meet the above demand, Tofflon works with his strategic partners and SME team to offer” Affordable Innovation Solutions” from technology transfer, WHO PQ Compliance Quality System Establishment to local manufacturing through innovative “Machinery + Modular Engineering + Value-Added Service for Bio-Technology Transfer” Solution. In the end, all our jointly developed “Affordable Innovation” will bring values to the ultimate benefit of our people.

This webinar will discuss three pivotal areas essential for successful technology transfer and local manufacturing: building a WHO-PQ compliant QA System, adhering to best practices in vaccine technology transfer, and utilizing innovative modular Drug Substance (DS) and Drug Product (DP) facilities for vaccine local manufacturing.


Speaker 1

Mr. Justin Khng

Senior cGMP Consulting Director, Tofflon Abioplus (a company of Tofflon Group)

Biography: Mr. Justin Khng has over 22 Years of experience both in China and Overseas. Undertaken positions with Fortune 500 Pharmaceutical companies and consulting companies specializing in Green Field Pharmaceutical Projects. Personally assisted numerous companies attained US FDA, EMA, PIC/s, WHO PQ GMP manufacturing license and status.

Speaker 2

Mr. Lokender Kaushik

Associate Director, Walvax Biotechnology

Biography: Mr. Lokender Kaushik, an expert in Quality Management Systems (QMS) and Good Manufacturing Practices (GMP), holds a Master’s degree in Science with extensive experience in the vaccine industry. He is skilled in leadership, quality audits, CAPA analysis, and regulatory compliance strategy. With a track record of achievements including managing a Bill & Melinda Gates Foundation (BMGF) funded WHO Prequalification (PQ) project, reducing technology transfer timelines by 30%, and setting up Quality Management Systems, Mr. Kaushik is a dynamic and motivated professional. In his current role, he provides high-level strategic and operational regulatory direction, oversees global regulatory submissions, and manages critical issues related to technology transfer and regulatory affairs.

Speaker 3

Mr. Zhichao Wang

Manager of Modular Engineering Department, Tofflon Group

Biography: Zhichao Wang, Manager at Tofflon Smart Engineering Co., Ltd., holds a master’s degree from Tianjin University. With expertise in designing and managing pharmaceutical projects, he understands biopharmaceutical processes, GMP, and building regulations. Wang established Tofflon’s Modular Engineering Department and developed modular factory projects, optimizing processes and ensuring compliance. He excels in modular factory construction and is recognized for innovation and industry influence.

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