Angela Psenicska

As a senior consultant and manager of the group’s Good Laboratory Practice (GLP)/Good Clinical Practice (GCP) Archiving Solutions, Angela Psenicska is responsible for the overall management of all services and the facility.  A seasoned specialist, she has been with the company for more than 25 years. Her past and current quality assurance (QA) experience covers all aspects of QA work under the Food and Drug Administration (FDA), Environmental Protection Agency (EPA) and Organisation for Economic Co-operation and Development (OECD) Good Laboratory Practice (GLP) regulations, plus FDA/International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Good Clinical Practices (GCP).

With more than 30 years of overall experience in the scientific research area, Ms. Psenicska previously worked as a research technician for the U.S. Army Medical Research Institute of Chemical Defense.  She also has served as a QA auditor at Biospherics Inc. and Amvax, Inc. facilities.  Additionally, she has been a Biological Safety Officer at Amvax, Inc.—responsible for the control of all biological organisms used in the company’s research and production facilities. Ms. Psenicska’s QA experience has included all study types (mammalian toxicology, ecotoxicology, biotechnology, analytical/bio-analytical chemistry, field trials, etc.) for regulatory submission. Her GCP experience involves her work with contract research organizations (CROs) and as principal investigator (PI) for site qualification audits, study site audits, database audits, report audits, etc.

She holds a B.S. degree from the University of Maryland Baltimore County.