Approvals and Clearances for Medical Devices conference will provide you with the knowledge and strategies to stay on top of the continuously evolving FDA guidelines. Last year, there were 700 incidents of MDR’s and 10 deaths. Consequently, FDA is becoming more stringent on these regulations. There’s too much at stake for you to miss this inaugural medical device approval event. Avoid risk, avoid recalls, and get your products to market quickly and cost effectively.
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V.P.‘s, Directors, Managers, Specialists and Consultants of: Regulatory Affairs, Corporate Affairs, Quality Assurance, Clinical Affairs, Quality Affairs, Quality Control, Regulatory Compliance.
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