As the Regulatory Affairs Manager, Rachael Hultman Vanderhoof ensures clinical research, pharmaceuticals and medical devices meet all guidelines set by regulatory agencies, such as the FDA. Rachael’s role involves planning and supervising regulatory actives for clinical trials throughout the entire lifecycle, managing essential documents, and acting as the main point of contact for government agencies.
Rachael guides the Regulatory Affairs team in following current laws and standards, avoiding compliance issues and providing strategic direction to keep research operations running smoothly and effectively.