Alford R Taylor emphasizes on risk management and CAPA measures. He is thorough and precise with his inspections, looking for detailed documentation and risk assessment protocols, particularly in device design constraints. His inspections highlight the importance of internal quality control measures.

FDA investigator Alford R Taylor is a vigilant and detail-oriented inspector whose primary focus is the quality systems associated with CAPA procedures, Management Review Procedures, Risk Reporting, Control of Non-conforming Products, Design Verification and Analysis. His reports consistently highlight the issues related to device design and specifications, risk management, and quality control. He prefers thorough evaluation of CAPA systems and risk assessments, favoring organizations that preemptively control all possible areas of risk.