Outsourced Pharma Capacity Update: Small Molecule API/HPAPI (free virtual event)

Leading CDMOs share their current available capacity – and associated capabilities, facility locations, and timelines – to help you identify options for your development and manufacturing needs.

The cornerstone of effective treatments lies in the quality and reliability of API production. Our event will spotlight the state-of-the-art facilities and cutting-edge equipment driving the API manufacturing process. Discover how the latest techniques ensure compliance, efficacy, and purity, from intricate chemical syntheses to stringent quality control measures. Learn about the pivotal role of scale-up strategies and environmental considerations in maintaining a sustainable and efficient production landscape.

What can you expect? – Short, digestible presentations with live interaction to give you an inside look at the available capacity of industry suppliers. You will have the opportunity to ask questions of each CDMO to better understand if they can meet your needs – all from the convenience of your computer!

Please note that this event is for biopharma companies seeking available capacity to connect with CDMOs who have that capacity available. Attendance is open to the following:

Individuals working for a pharma or biotech company with an active therapeutic pipeline.
Industry consultants and capital investment firms.
CDMO sponsors of the event.