The speaker also will review the important role of quality assurance in HPAPI manufacturing and delve into the questions you should ask a CDMO about their capabilities and corporate commitment to processing these complex APIs.
TORONTO (PRWEB) November 26, 2019
The live webinar taking place on Tuesday, December 17, 2019 at 11am EST (4pm GMT) will discuss the value of different types of containment technology, the significance of protocol during equipment changeovers and the advantages of certain cleaning strategies. The speaker also will review the important role of quality assurance in HPAPI manufacturing and delve into the questions you should ask a CDMO about their capabilities and corporate commitment to processing these complex APIs.
Are you looking for the right contract development and manufacturing organization (CDMO) to develop and manufacture your high potency active pharmaceutical ingredients (HPAPIs)? Or have you been unsure about the CDMO you’re currently working with?
Join industry expert Brian P. Haney, PhD, Director of Technical Operations at AMRI to learn what answers to look for and be prepared to spot the red flags that could add major risk to their critical projects.
For more information or to register for this event, visit Choosing the Right CDMO for HPAPI Development & Manufacturing.
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