One award available.
Five hours of regulatory support to refine the awardee’s U.S. regulatory strategy. A senior regulatory leader at Veranex will meet with the company to gain an understanding of their technology, Intended Use, Indications for Use, and aspirational claims. Veranex will provide advisement and thought partnership to guide the team’s U.S. FDA regulatory pathway for device commercialization.
Veranex is a full service, end-to-end global medical device consulting firm and solutions provider, offering support with product design/development/engineering, preclinical studies, human factors, regulatory affairs, quality systems, clinical trial strategy/execution and data management, and reimbursement strategy through to successful market access. We help early-stage medical device companies advance innovation, fueled by our deep understanding of unmet market needs — from clinician to payer to patient — and our exceptional expertise.