In moving through the CMC development cycle, it is important to prospectively identify where there may be knowledge gaps and to create studies to address them.
TORONTO (PRWEB)
June 24, 2021
Successful biopharmaceutical Chemistry, Manufacturing and Controls (CMC) development requires a clear understanding of the requirements and expectations to support taking a product into the clinic. Even after the product has entered the clinic the CMC development journey continues.
In moving through the CMC development cycle, it is important to prospectively identify where there may be knowledge gaps and to create studies to address them. Risk management is used to build robustness and contingencies into the process development plan. It is also essential to look at where compromises and trade-offs are in the process development approach.
Register for this webinar to hear a discussion about how to structure a biopharmaceutical process development program to build supporting data as the product progresses in the clinic. It will touch upon gaining understanding of the key quality attributes and critical process parameters as part of developing the process. This includes methodology that takes a holistic approach to process development. The discussion will also cover the importance of generating product and process intermediate stability data as part of the CMC package.
Additionally, the discussion will touch upon how developing process robustness while also managing resources is a key success factor. To explore this concept, there will be an overview of how to define the “good enough” areas in process development, where 80 percent may be good enough and where it may not. It will also include where and when it makes sense to leverage platform data in process development.
Join Louise Duffy, SVP, Scientific Project Leaders, Abzena, for the live webinar on Wednesday, July 14, 2021 at 10am EDT (3pm BST/UK).
For more information, or to register for this event, visit Process Development: Getting from Phase I to III.
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