Enabling MedTech Professionals
to move beyond documentation
What does VidyaRA do?
VidyaRA works at the intersection of Regulatory Affairs education, technical advisory, and capability building for MedTech professionals around the world.
VidyaRA enables professionals and teams to engage with regulatory requirements with greater clarity and intent, toward stronger regulatory thinking over time.
Leadership behind VidyaRA
VidyaRA is founded by Heena Thakkar, a certified Regulatory Affairs professional (RCC-MDR, MS in Regulatory Affairs) with experience across global regulatory frameworks, including hands-on involvement with EU MDR evolution since its inception.
Having worked closely with organizations and cross-functional teams in both the United States and India, she observed a recurring gap in regulatory understanding, confidence, and decision-making. VidyaRA was created to address this gap through education, advisory-led consulting, and capability building.
Her work today focuses on enabling MedTech professionals and teams to move beyond documentation-led approaches and develop stronger regulatory thinking over time.
Fundamentals-first Trainings for MedTech Professionals
Technical support and capability-building engagements for enterprises
