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Devices and Diagnostics Consulting Group (DDCG) is a professional services firm that provides regulatory, quality, and clinical consulting to the medical device and diagnostic industries. Founded in 1999, the company specializes in helping clients navigate the regulatory requirements for the FDA, European Union (MDR/IVDR), and other international markets. Their expertise includes 510(k) and PMA submissions, Quality Management System (QMS) development, and clinical study management. DDCG supports a wide array of healthcare technologies, ranging from simple Class I devices to complex Class III life-sustaining systems. The firm also provides auditing services and post-market compliance support to ensure ongoing adherence to global standards. By leveraging deep industry experience, DDCG assists both startups and established firms in accelerating their path to commercialization.
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