Alexis Stroud's career included serving as Validation Scientist for CSSC, a compliance consulting company, conducting computerized system validation, regulatory training, 21 CFR Part 11 assessments, equipment qualification, quality system development, and auditing for over 30 life science companies. Ms. Stroud currently directs the Quality and Compliance Department for QPharma, Inc., a service provider in the life science and related industries offering a wide range of regulatory and compliance solutions. QPharma’s suite of professional services spans the product development lifecycle, from quality and validation solutions to PDMA and fulfillment services. Ms. Stroud specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management. She has completed more than 180 software validation projects for numerous regulatory systems including SFA, SAS, WMS, LIMS, BMS, and QMS.