2025
TBD
Daniel Walter is a Policy Analyst in the Center for Devices and Radiological Health (CDRH), FDA, as a member of the Case for Quality. The Case for Quality is an ongoing strategic priority for CDRH to improve access and outcomes for patients and improve device quality by engaging industry, payers, providers, and patients to focus on the quality and performance of medical devices.
Daniel has been with the FDA working in compliance and supporting the Total Product Lifecycle for over 15 years, including as a supervisor for 10 years, with a broad experience that covers many device fields and regulatory scenarios. Daniel joined the Case for Quality team in 2020. Prior to working with FDA, Daniel was a Validation Engineer for several contractors in the pharmaceutical industry, which lead to becoming a Lead Quality Auditor and Director of Quality before joining FDA.
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