Office of Rare Diseases Research
The Office of Rare Diseases Research is a division of the US National Center for Advancing Translational Sciences (NCATS) that oversees the Rare Diseases Clinical Research Network and Genetic and Rare Diseases Information Center.[1]
File:Anne R. Pariser.jpg
Anne R. Pariser, M.D., Director of the Office of Rare Diseases Research
History
The Office of Rare Diseases Research was established in 1993 within the Office of the Director of the NIH. Its responsibilities were mandated by statute by the Rare Diseases Act of 2002.[2][3] In 2011, the office became part of the newly created NCATS.[4] ORDR is currently headed by Dr. Anne R. Pariser, who took over the position in February 2018.[5]
References
- ↑ "Divisions & Offices". National Institutes of Health. https://ncats.nih.gov/about/center/org. Retrieved 8 July 2018.
- ↑ "The Office of Rare Diseases Research (ORDR)". https://www.rarediseasesnetwork.org/spotlight/spring2011/ORDR/index.htm. Retrieved 8 July 2018.
- ↑ "Office of Rare Diseases Research (ORDR) Brochure". National Institutes of Health. https://rarediseases.info.nih.gov/asp/resources/ord_brochure.html. Retrieved 8 July 2018.
- ↑ "Kaufmann Appointed Head of NCATS' Office of Rare Diseases Research" (Press release). National Institutes of Health. September 2015. https://ncats.nih.gov/news/releases/2015/ordr-director. Retrieved 8 July 2018.
- ↑ "Staff Profile: Anne R. Pariser". https://ncats.nih.gov/staff/pariserar.