Navigating 510(k) and PMA Submissions and Approvals 2011

This premier marcus evans conference will address potential regulatory changes in the PMA and 510(k) submission and approval process and provide regulatory affairs executives knowledge on how to streamline their submission process by anticipating FDA requirements. Attendees will also increase their knowledge base in efficient submission documents, identify potential pitfalls in data that could delay approvals and obtain a rapid approval for their products to be approved.