Module 9 2021
16/03/2021
Specific Module 3 Components (cont.)
3.2.S.2.5 Process Validation ● SM – typically not applicable
● Biotech – considerably more complex section which evolves as a program develops. Essentially you need to provide sufficient information to demonstrate appropriate validation and evaluation of the manufacturing process for the stage of development of your product
The Organisation for Professionals in Regulatory Affairs
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Specific Module 3 Components (cont.)
3.2.S.2.6 Manufacturing Process Development – Critical section for justifying applicability of your current/future manufacturing process to what was used in previous clinical studies – SM – typically not extensive – Biotech – considerably more complex section which needs to clearly assess the impact of each manufacturing change through product development on the drug substance and drug product which can include specific nonclinical or clinical studies
The Organisation for Professionals in Regulatory Affairs
16
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