Pearl Pathways is a comprehensive life science regulatory, quality compliance, and clinical services consulting company providing strategic guidance and project-based support for emerging to mid-size biopharmaceutical, medical device, and diagnostic companies.
Pearl Pathways can provide the expertise, bandwidth, and flexibility to help you define or drive your product development strategy. Our clinical, scientific, industry, FDA and global regulatory authority experience helps our clients successfully navigate a highly complex regulatory environment while balancing risk, speed to market, and cost to achieve their business goals. Pearl Pathways supports all aspects of human research through its full-service central independent review board, Pearl IRB.