Merry Christie adopts a methodical and thorough approach, meticulously analyzing documentation, processes, and procedures to ensure accuracy and compliance. He places a strong emphasis on adherence to regulatory standards and best practices, particularly in areas related to discrepancies, quality control, and deviation management.

Merry Christie is a detail-oriented FDA auditor with a strong focus on discrepancies in manufacturing processes, inadequate quality assurance policies, and deficiencies in handling in-process samples and microbial control measures. He prioritizes accuracy and compliance in Quality Control testing procedures, Out-of-Specification events, and bioburden sampling. Merry Christie tends to scrutinize deviation handling procedures and justifications for delays, emphasizing timeliness and appropriate reasoning.