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Hany Demian
FDA Standards Executive, Office of the Chief Scientist, Office of the Commissioner
Hany Demian is a prominent figure in the field of medical device regulation and standardization, currently serving as the Standards Executive at the U.S. Food and Drug Administration (FDA).15 With over 26 years of experience at the FDA, Demian has made significant contributions to the development and implementation of consensus standards in the medical device industry.2
Professional Background
Demian's extensive career at the FDA includes 22 years of experience in the Center for Devices and Radiological Health (CDRH), where he focused on premarket review of medical devices.2 This background has provided him with deep insights into the regulatory processes and challenges faced by medical device manufacturers.
Achievements and Recognition
In 2018, Hany Demian was awarded the prestigious Robert J. Painter Award, which honors outstanding leaders in the field of standardization.14 This recognition underscores his significant contributions to the development and promotion of consensus standards in the medical device industry.
Current Role and Responsibilities
As the FDA's Standards Executive, Demian plays a crucial role in:
- Overseeing the development and implementation of consensus standards for medical devices
- Representing the FDA in various standardization committees and initiatives
- Collaborating with industry stakeholders to improve the safety and effectiveness of medical devices
Professional Network
Hany Demian maintains an active presence on professional networking platforms, with a LinkedIn profile under the username hany-demian-37797828.3 This allows him to connect with other professionals in the field and share his expertise on regulatory science and innovation.
Through his work at the FDA and his contributions to standardization efforts, Hany Demian continues to play a vital role in shaping the regulatory landscape for medical devices and advancing patient safety.
