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LumiPath

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LumiPath™ by Luminari is an AI platform that simplifies clinical protocol development and regulatory document preparation for sponsors and CROs. Built on more than 10,000 regulatory documents and aligned with FDA, EMA and ICH requirements, LumiPath helps teams develop structured drafts for expert review, improve consistency across documents and streamline revisions. Teams bring their study objectives, supporting information and prior documents into LumiPath to develop a structured protocol draft. Clinical and regulatory experts review the content, resolve questions and direct revisions, keeping responsibility for scientific judgment and final approval. The result is less manual drafting and more time for science, strategy and the decisions that advance development.

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