We’re leveraging our team’s expertise in clinical trial innovation, recognizing that optimal human outcomes stem from the collaboration of well-equipped individuals and revolutionary ideas. That’s why we provide the enabling technology that drives RBQM and data quality oversight, as well as comprehensive support in business and clinical acumen, ensuring our partners have the necessary tools and knowledge for success in clinical research.
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Aligned with guidance from all major global regulatory bodies, including the FDA, EMA, MHRA, and PDMA, CluePoints is fully compliant with Good Clinical Practice (GCP) guidelines. Our AI-powered, risk-based execution strategies enable the life sciences industry to achieve ongoing ICH and ISO compliance while focusing on what matters most.
Site Profile & Oversight Tool (SPOT) and Intelligent Medical Coding (IMC) unveiled by RBQM innovator at DIA Global Annual Meeting 2024 King of Prussia, PA –