Wedgewood Pharmacy LLC applied for registration as an importer of controlled substances with the Drug Enforcement Administration.
NIH submits its Extramural Harassment Web Form for OMB review under the Paperwork Reduction Act, with a 30-day public comment period.
The National Cancer Institute offers licensing of the A1847 human ovarian carcinoma cell line, a BRCA1-deficient model for researchers studying cell cycle regulation, tumor suppression, and DNA damage repair drugs.
DOJ's Office of Justice Programs seeks OMB approval for a new information collection on T visa certification letter requests; public comments accepted through the Federal Register notice period.
Center for Scientific Review will hold closed meetings to review grant applications and personnel matters; specific dates and locations available upon request to the designated agency contact.
National Institute of Diabetes and Digestive and Kidney Diseases announces an amended meeting notice for its advisory council to discuss research priorities and funding initiatives affecting small biotech and life-sciences firms.
Center for Scientific Review announces amended open meeting schedule to discuss peer review processes and grant evaluation procedures for National Institutes of Health funding cycles.
National Institute on Aging offers licensing opportunities for fluorophthalimide compounds in development as anti-inflammatory therapeutics for systemic and neurodegenerative disorders.
Veranova, L.P. has applied for DEA registration as a bulk manufacturer of controlled substances; supplementary drug information is available in regulatory notices.
Cerilliant Corporation seeks DEA registration as an importer of controlled substances; refer to supplementary information for specific drug classes.
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