CRED Managing Variations Effectively

Chapter B – Post approval change management protocol

Examples of CMP submissions received: • Introduction of additional manufacturing site for FP/ AS, • Introduction of a new purification cartridge • Changes in reprocessing of certain steps in manufacturing process of AS • Scale up of manufacturing of Active substance (biological) • Changes to in-process control testing strategy

Protocol included in 3.2.R

Introduction to Classification of CMC (Quality) / Clinical / PhV Variations 60

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