Angela Psenicska is a Senior Consultant and Manager of the QAI GLP Archive Facility. She has been with QAI for over 25 years. Ms. Psenicska is responsible for the overall management of the QAI GLP Archive. She has more than 30 years of experience in the scientific research area.
Her past and current quality assurance (QA) experience covers all aspects of QA work under the FDA, EPA, and OECD Good Laboratory Practice (GLP) regulations, plus FDA/ICH Good Clinical Practices (GCP).
Prior to joining QAI, Ms. Psenicska worked as a Research Technician for the US Army Medical Research Institute of Chemical Defense, then as a Quality Assurance Auditor at Biospheric’s, Inc. and Amvax, Inc. She also served as a Biological Safety Officer at Amvax Inc., responsible for control of all biological organisms used in the research and production facilities.
Ms. Psenicska quality assurance experience has included all study types (mammalian toxicology, ecotoxicology, biotechnology, analytical/bio-analytical chemistry, field trials, etc.) for regulatory submission. Her GCP experience involves CRO and PI site qualification audits, study site audits, database audits, report audits, etc.
Ms. Psenicska holds a bachelor’s degree from the University of Maryland Baltimore County.