Arista

Arista emphasizes on the validation of the sterilization process and environmental monitoring, giving these areas a thorough review. He is also attentive in inspecting the aseptic processing areas to make sure they are up to standard. For him, discrepancy in batch production records is a major red flag and suggests sloppy work and potential risks to product safety. He enforces strict adherence to written procedures.

FDA Auditor 'Arista' appears to show a strong focus on the validation of sterilization processes, environmental monitoring programs, aseptic processing areas, review of batch production records and adequacy of written procedures. Arista is detail-oriented and stringent when it comes to all aspects of sterilization, contamination prevention, and adherence to documented procedures.