Allison V Bonnenburg
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Detailed Analysis
Allison V Bonnenburg meticulously scrutinizes the testing and validation processes, cleanliness, and facility management related to sterile drug manufacturing. She places a strong emphasis on documentation and adherence to quality control procedures throughout the manufacturing and change control processes.
Allison V Bonnenburg is a detail-oriented FDA investigator who is particularly focused on the quality control and cleanliness of sterile drug manufacturing processes. She prioritizes thorough testing and validation of components, batch manufacturing processes, and cleaning procedures. Additionally, she places a significant emphasis on facility management and change control procedures to maintain the quality of sterile drugs.
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