Elizabeth M. Troll is a seasoned executive with over 42 years of global leadership in quality assurance, regulatory compliance, and governance within the pharmaceutical, biopharmaceutical, and healthcare industries. Renowned for her expertise in Quality Management Systems (QMS), vendor oversight, inspection readiness, and leadership development, Liz has played a pivotal role in shaping compliance frameworks that align regulatory standards with business efficiency. She has led quality and compliance initiatives at Endpoint Clinical, Novan Inc., QuintilesIMS, and Otsuka, driving strategic improvements and fostering a culture of operational excellence. A dynamic speaker and mentor, Liz is passionate about developing future leaders, advancing industry best practices, and supporting organizations in achieving regulatory success. With a strong commitment to integrity, respect, and continuous improvement, she seeks to leverage her expertise through board service and advisory roles, helping companies navigate complex regulatory landscapes and drive sustainable growth.

Frank Pokrop is an accomplished leader in regulatory affairs and quality assurance, bringing over 15 years of expertise across medical devices, software/SaMD, capital equipment, and injectable drugs. Certified in multiple disciplines, including RAC, CQE, CQA, CSQE, and CPGP, he has successfully navigated complex global regulatory landscapes, overseeing product approvals and quality management systems for leading organizations such as Abbott, BD, CareFusion, and QuidelOrtho. Renowned for his strategic mindset and collaborative approach, Frank has led global compliance programs across 48 sites, driven cost reductions exceeding $3 million annually, and served as a trusted regulatory liaison for corporate boards and international agencies. A results-oriented executive with a passion for developing teams and achieving excellence, Frank is now seeking a senior position in regulatory affairs or quality assurance to further his impactful career.