For pharmaceutical and biopharmceutical companies with products in development, DSI is the CMC and regulatory affairs company to partner with.
DSI specializes in providing regulatory, product development and quality systems consulting services. Our staff consists of experts in quality management, regulatory affairs, product manufacturing and testing, statistics, and GMP, GCP regulatory compliance. We offer consulting services and regulatory support based on a full understanding of FDA regulatory expectations and policies.
DSI can drive your product development program from start to finish. Or, fill in-house CMC expertise gaps on a project basis.