Rachel North is an experienced Regulatory Affairs professional with an efficient, collaborative approach to navigating the regulatory landscape.
She has broad experience with Class I-III medical device companies and healthcare government affairs.
Achieving regulatory success requires high-quality submissions by translating complex information, anticipating feedback, and developing productive relationships with regulators and functional area experts.
North MedTech provides a variety of Regulatory Affairs and Quality System services. Our efficient, practical approach aligns business strategy with global regulatory requirements to establish and maintain product marketability.
©2021 North MedTech
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