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Dana Lagman


Dana is an accomplished professional with expertise in clinical trials and biomedical manufacturing. She excels in maintaining and managing documentation for clinical trials, writing and reviewing protocols, and overseeing auditable clinical trial files. 


Dana specializes in implementing clinical trials and research activities for IVD assays, coordinating study materials, and ensuring accurate data reporting. She possesses strong communication skills and proficiency in adhering to GMP/GLP guidelines, FDA regulations, and ISO/EU standards. 


As a Quality Assurance II Specialist/Biomedical Manufacturing Associate II, Dana handled various quality-related responsibilities, including NCMRs, CAPAs, and document control. 


She holds a Bachelor of Science in Biochemistry from California State University of East Bay and is certified in Good Clinical Practice and ISO 13485:2016 Auditing. Dana's work reflects a highly motivated and responsible attitude with a positive approach to getting the job done.

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