HPAPIs are a rapidly expanding group of therapeutics due to the recent commercial approvals of 8 ADCs and other targeted therapies. As the potency of these new compounds increases, API manufacturers are challenged to evolve their equipment, facilities, and processes to keep up with the industry.
In recent years, the pharmaceutical industry has been moving toward drugs with increasing potency, including ones with OELs in the single nanograms/m³. This shift is occurring as a result of better-targeted therapies in the oncology space as well as due to more toxicological data about previously approved APIs. With much of this work being outsourced, many contract manufacturing organizations wishing to operate in this field have had to update their processes to handle these materials and ensure the safety of their operators. In this presentation, we will show how MilliporeSigma has met these challenges and is preparing to lead in this area moving forward.
In this webinar, you will learn:
- the evolution of the high potent API manufacturing industry from 10 µg to single nanogram limits
- different safety concepts to handle highly potent compounds
- about the most commonly used payload classes in the ADC field
Speaker
John Stevens
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Field Marketing Manager
John Stevens joined the company in 2004 and held a variety of positions in our HPAPI facility, focusing on project leadership in the scale up and first-time GMP production of HPAPIs and complex APIs and lead the site MSAT team for 3 years. In 2019 he took on a role as a field marketing senior specialist for the actives & formulation team. Currently, John supports the life science services commercial team in the small molecule modality. John received his M.S. in chemistry from the University of Wisconsin.
Pharma and biopharma manufacturing
- Antibody drug conjugate manufacturing
Duración:38min
Idioma:English
Sesión 1:presentado May 25, 2022
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