Quality and Regulatory

Ms. Garg works at the intersection of quality systems, regulatory strategy, and software-driven medical devices, with a particular focus on UX/UI considerations in clinical software. With a strong foundation in bioengineering and medical product development, she supports compliant, user-centered design and documentation across the software lifecycle. Her background includes extensive research experience in women’s health and regulatory exposure through engineering-focused legal work, bringing both technical rigor and patient-impact awareness to her role at Aneurisk.

She is currently pursuing her Master’s in Medical Product Engineering, building on two years of research experience in pelvic organ prolapse at UPMC Magee and a two-year internship with the engineering law firm Belles Group in Philadelphia.