Kellie L Thommes
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Detailed Analysis
Kellie L Thommes is thorough and meticulous. She pays close attention to the procedures and protocols involved in clinical investigations, with particular focus on maintaining investigational drug records, submission procedures for IND applications, and the informed consent process.
Kellie L Thommes is a keen FDA investigator with high penchant for regulatory adherence. His primary attention lies in the compliance with the submission of Investigational New Drug applications, securing informed consent, timely reporting of events as per the investigational plan and maintaining complete investigational drug records. He also detests any unauthorized changes in the research activity.
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