Sustainability is critical in pharmaceutical manufacturing, especially in Active Pharmaceutical Ingredient (API) production, which significantly impacts global emissions.
This webinar addresses the sustainability challenges and evolving needs in small molecule API manufacturing, showcasing how regulatory pressures drive change. Join industry experts as they share compelling case studies that highlight the principles of green chemistry and innovative manufacturing techniques. Discover practical approaches for enhancing sustainability in chemical process design and learn how successful optimizations align with our commitment to sustainability as a leading small molecule API CDMO.
In this webinar, you will learn about the:
- economic viability of designing for sustainability
- tools for calculating PMI and carbon footprint on your processes
- impact of novel technologies, such as flow chemistry
- real case studies showing improved PMI and carbon footprint scoring
Speakers

Andrea Wong
Merck
Manager, Process Development
Andrea is currently a manager in process development at the Madison, WI site. An organic chemist by training, she spent many years in the lab before changing roles to manage a team of chemists. She is experienced in process transfer for antibody-drug conjugate programs and small molecule APIs. After training for a graduate degree in asymmetric epoxidation, Andrea did post-doctoral work in the field of gold nanoparticle synthesis.

Robert Minkebige
Merck
Associate Director, R&D
Robert is an associate director of R&D, working on new process technology including processing equipment, simulation software, and data acquisition projects that drive efficiency and capacity. Starting at our Sheboygan site and later transitioning to Madison’s HPAPI location, he has worked on improving chemical processes for 7 years after receiving his B.S. in chemical engineering from Case Western Reserve University.

Tobias Haag, Ph.D.
Merck
Director Process and Analytical Development
Tobias is a director of process and analytical development at our center of excellence for drug delivery compounds in Schaffhausen, Switzerland. With 20+ years of experience in the pharmaceutical industry, Tobias leverages his broad expertise in process development, technology transfers, scale-up, GMP manufacturing, analytical development and project management to support our CDMO service offerings. He holds a doctoral degree in Chemistry from the University of Konstanz, Germany.

Bertram Cezanne, Ph.D.
Merck
Department Head of Process Development
Bertram Cezanne heads process development synthesis within the electronics business of Merck. A chemist by training, he holds a Ph.D. in synthetic organic chemistry. In 1997, he joined Merck and worked for more than 15 years in drug discovery and early scale-up, where he gained broad experience in synthetic organic chemistry at different scales. Since 2016, he has been responsible for process development and supply of APIs, intermediates, and excipients during the development phase until launch and commercial manufacturing.
Pharma and biopharma manufacturing
- Pharma and biopharma manufacturing
期间:1h
语言:English
场次 1:Thu, July 10, 2025 4:00 PM CEST
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