The approach of Suball Chaudatte D Brooks seems to be methodical, detail-oriented, and strongly focused on compliance with standard operating procedures and regulatory requirements. He also stresses on thorough documentation and effective processes to assure product quality and safety.

FDA Auditor Suball Chaudatte D Brooks appears to have a keen eye for product design and validation processes, prioritizing thoroughness over rushing to market launch. He also shows a significant interest in complaint handling, auditing procedures, and ensuring all alterations and deviations in validated processes are correctly documented. Environmental factors like cleanliness, temperature conditions, and contamination prevention seem to be significant areas of interest. He seems to value thorough documentation and adherence to standard operating procedures (SOPs). He also appears to prioritize regulatory compliance, particularly regarding Medical Device Reporting (MDR) and market withdrawal reporting.