Motivated MSRA student with coursework in regulatory science, quality management, and medical device pathways (510(k), CE). Skilled at translating regulatory requirements into practical steps, conducting literature and guidance reviews, and supporting documentation for submissions. Actively seeking internships and mentorship to build experience in dossier preparation, labeling, and post‑market compliance. Committed to lifelong learning, professional development through RAPS, and contributing to patient‑centered product access.