I'm a Regulatory Labeling Professional with deep expertise in the medical device and healthcare industries—where clarity, compliance, and precision are non-negotiable. I lead cross-functional labeling initiatives that align with global regulatory standards (FDA, EU MDR, ISO) while ensuring clear, accurate, and user-centric content across IFUs, product labels, and packaging artwork.

 

I’ve successfully driven complex global label change projects, led end-to-end rebranding efforts, and implemented scalable processes that enhance quality, traceability, and speed to market.

 

My core strength lies in bridging regulatory rigor with practical execution. I translate complex requirements into clear, actionable guidance—aligning regulatory, quality, and product development teams to support collaboration, compliance, and patient safety throughout the product lifecycle.