SciLucent, Inc.
Melanie Bell is an experienced professional in the field of regulatory affairs and product development, currently serving as Principal Consultant at SciLucent, Inc. since March 2013, where responsibilities include project management for integrated product development programs and CMC technical review. Prior roles encompass Regulatory Specialist II at Technical Resources International, Inc., with extensive expertise in preparing and submitting regulatory documents for clinical studies, and Regulatory Associate at CROfessionals, where submission preparations to regulatory agencies were key activities. Further experience includes a role as Sr. Associate Development at Metastatix, focusing on IND preparation and contract research management, and an independent consulting role assessing intellectual property landscapes. Melanie holds a Master of Science in Bioscience and Regulatory Affairs from Keck Graduate Institute and a Bachelor of Science in Genetics from The University of Georgia.
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SciLucent, Inc.
SciLucent provides FDA-focused regulatory, clinical, nonclinical, CMC, quality, scientific, and management consulting services to healthcare product companies that develop, manufacture and/or market pharmaceuticals, biopharmaceuticals, medical devices, combination products, and dietary supplement ingredients. Since 1998 we have provided our clients with innovative strategies and exceptional quality work products intended to enhance product development, approval, and marketing presence.