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"I had the pleasure of managing Ri in regulatory documentation. She brought exceptional rigor and structure to literature evaluation and documentation development, expertly identifying high-quality regulatory-grade studies using strong epidemiological and statistical principles. Her reviews of clinical outcomes and safety data were consistently balanced, guideline-aligned, and scientifically sound. Ri worked independently through complex regulatory reviews, delivering precise data verification, scientific integrity, and clear communication in cross-functional collaborations."

Maggie Farhat, MS, Manager of Scientific/ Clinical Affairs, Johnson & Johnson MedTech

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