Gender: Female
Sousan S. Altaie is Scientific Policy Advisor for the Office of In Vitro Diagnostic Devices in the United States. She joined the Food and Drug Administration in the Center for Drug Evaluation and Research in the Division of Anti-infective Drug Products as a primary reviewer in 1995. Six years later she joined the FDA's Center for Devices and Radiological Health as the Chief of Immunology and Molecular Diagnostics Branch. She is actively working as a member of the Global Harmonization Task Force (GHTF) and International Organization for Standardization (ISO) working groups. She was appointed the CDRH Critical Path Coordinator in 2004 and is actively involved in the Agency's Critical Path initiative. She has served as an observer, advisor and full member of various committees and subcommittees of the Clinical and Laboratory Standards Institute (CLSI).
Source: Wikipedia | Last updated on May 16, 2024
On the name Sousan S. Altaie, Sousan means Lily of the Valley.
The name Sousan S. Altaie is often used as a Female name and is mostly used as a First Name.
Sousan is commonly found in Morocco, Iran, United States of America, and 38 more countries.
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At NamesLook, the name Sousan is recorded 489 times globally, ranking it as the 58,380th most common name worldwide.
Sousan is most prevalent in Morocco, with 66 occurrences, making it the 11,443th most popular name in the country.
In Iran, the name Sousan is found among 1 in every 2839 people, showcasing its highest frequency there.
| Country | Rank | Frequency |
|---|---|---|
| Morocco | #11,443 | 1 : 15,955 |
| Iran | #3,130 | 1 : 2,839 |
| United States of America | #26,736 | 1 : 33,502 |
| Syrian Arab Republic | #8,809 | 1 : 10,238 |
| Algeria | #18,443 | 1 : 35,012 |
| Canada | #9,947 | 1 : 12,373 |
Sousan S. Altaie is Scientific Policy Advisor for the Office of In Vitro Diagnostic Devices in the United States. She joined the Food and Drug Administration in the Center for Drug Evaluation and Research in the Division of Anti-infective Drug Products as a primary reviewer in 1995. Six years later she joined the FDA's Center for Devices and Radiological Health as the Chief of Immunology and Molecular Diagnostics Branch. She is actively working as a member of the Global Harmonization Task Force (GHTF) and International Organization for Standardization (ISO) working groups. She was appointed the CDRH Critical Path Coordinator in 2004 and is actively involved in the Agency's Critical Path initiative. She has served as an observer, advisor and full member of various committees and subcommittees of the Clinical and Laboratory Standards Institute (CLSI).
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