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Our team has built an established reputation by working to streamline the effectiveness and success of clinical trials for over a decade, advising across every stage of the process – from site qualification to post commercialization.

MCRA is the leading U.S. Regulatory Advisor for the Medical Device and Biologics industries. Our deep bench of talent in virtually every discipline creates value and mitigates risk by combining  unparalleled comprehension of FDA laws and regulations. MCRA both advises and implements all types of strategies and FDA submissions.

Our expansive experience with international regulatory bodies across a number of device technologies enables us to help clients operate, expand, and achieve long-term business objectives in global markets.

MCRA’s reimbursement experts guide leading healthcare companies through the most complex dynamic in medical technology commercialization today.

We understand that medical device companies must adhere to strict FDA and international quality assurance requirements to ensure product consistency and safety. Our quality assurance team combines their in-depth knowledge to cover the nuances of this complex area.

MCRAs Compliance Services are designed to support the growing healthcare organization or medical device company that knows an effective Corporate Compliance Program is an essential business requirement in today's complex legal and regulatory environment.

With the continued advancement in technology and medical devices, MCRA's cybersecurity experts provide full integrated services to secure and protect your medical device by leading the discussions and delivering thorough risk assessments, strategy, and advisory services.

Lorem ipsum dolor sit amet, consectetur adipiscing elit. In egestas maximus justo. Cras auctor mi a ultrices congue. Vestibulum fringilla sollicitudin massa, et iaculis nisl rutrum vitae. Morbi porta mauris quis pretium eleifend.