Office of Immunology and Inflammation (OII)
The Office of Immunology and Inflammation (OII) consists of six review divisions:
- Division of Dermatology and Dentistry (DDD)
- Division of Gastroenterology (DG)
- Division of Hepatology and Nutrition (DHN)
- Division of Pulmonology, Allergy and Critical Care (DPACC)
- Division of Rheumatology and Transplant Medicine (DRTM)
- Division of Pharm-Tox for Immunology and Inflammation (DPT-II)
The Immediate office oversees the development, review, and regulation of applications for drug and biologic products reviewed in these divisions.
The staff of OII consists of highly trained physicians, scientists and regulatory project managers with expertise in gastroenterology, dermatology, dental, hepatology and nutrition, metabolism, pulmonology, allergy and critical care, and rheumatology and transplant medicine, pharmacology/toxicology, and regulatory affairs. These professionals work with specialists in other CDER scientific disciplines such as statistics, clinical pharmacology, epidemiology, chemistry, and drug safety to collaboratively review data on new treatments.
OII is committed to facilitating rapid development, review, and action on promising new therapies. Scientists within the office are working intensively on incorporating innovations in pharmacogenomics, bioinformatics, and clinical trial design into the drug development process.
- Physician Request for a Single Patient IND for Compassionate or Emergency Use
- Investigator-Initiated Investigational New Drug (IND) Applications
- Meetings and Workshops
- Guidance Documents
- Drug Safety and Availability
Contact Us
Mailing Address:
Food and Drug Administration
Center for Drug Evaluation and Research
Office of Immunology and Inflammation
10903 New Hampshire Avenue, Silver Spring, MD 20993
Building 22, Suite 4177
Phone: (301) 796-2240
Fax: (301) 796-9838
Resources
- Office of New Drugs
- CDER Offices and Divisions
- Reorganization of the Office of New Drugs with Corresponding Changes to the Office of Translational Sciences and the Office of Pharmaceutical Quality