Laura Boll

Laura Boll has extensive experience in regulatory affairs and quality management. Laura began their career at Medovations, Inc. in 2003 as an Engineering Manager and worked their way up to become the Vice President of Regulatory Affairs and Quality. Laura also held various roles at Medovations, including Director of Quality and Regulatory Affairs, Senior Manager of Quality and Regulatory Affairs, and Manager of Quality Engineering. In 2014, they joined Sandhill Scientific, a Medovations Company, as the Vice President of Regulatory Affairs and Quality. In 2017, Laura Boll moved to Diversatek, Inc. where they currently hold the position of Vice President of Regulatory Affairs and Quality.

Laura Boll attended the Milwaukee School of Engineering from 1988 to 1993, but the degree and field of study are not provided. Laura obtained several certifications in recent years, including "CE Mark Technical Documentation: Changes, Application, and Notified Body Expectations under MDR" and "Effective Post-market Surveillance in the EU under MDR" from Greenlight Guru in 2021, as well as "Essentials for Clinical Evaluation of Medical Devices," "How to Maintain a QMS Compliant to MDR & IVDR," and "How to Prepare for Common MDR Audit Pitfalls" also from Greenlight Guru in the year 2021. In 2018, Laura Boll achieved the certification of ASGE Recognized Industry Associate (ARIA) from the American Society for Gastrointestinal Endoscopy (ASGE).