Cheryl A Clausen
Visit Investigator ProfileInvestigation Details
Detailed Analysis
Cheryl A Clausen prioritizes the scientific rigor and compliance of batch failure investigations, production records, and laboratory practices. She pays close attention to consistency and completeness in testing procedures and the adherence to quality unit procedures. Additionally, she scrutinizes the appropriateness of equipment design for drug product manufacturing and storage.
Cheryl A Clausen tends to focus on the thoroughness and scientific soundness of batch failure investigation, documentation of production processes, completeness of laboratory records, compliance with test procedures, examination and storage of reserve samples, determination prior to product release, quality unit adherence to procedures, and equipment design.
Unlock Insights from 483s & Stay Audit Ready with FDA Tracker
Monitor FDA Six Systems, Analyse 483s with Observations, Investigators & Companies