Wedgewood Pharmacy LLC applied for registration as an importer of controlled substances with the Drug Enforcement Administration.
Proposed rule codifies Medicare Drug Price Negotiation Program under the Inflation Reduction Act of 2022 and establishes new policies for drug benefit programs and fixed combination drugs.
Medicare's final rule strengthens oversight of accrediting organizations by addressing conflicts of interest, establishing consistent standards, and updating validation systems for deemed providers and suppliers across multiple care settings.
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.
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.
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.
CMS is soliciting public comments on proposed information collection activities under the Paperwork Reduction Act; interested parties may submit feedback on burden estimates and collection methodology.
NIH submits its Extramural Harassment Web Form for OMB review under the Paperwork Reduction Act, with a 30-day public comment period.
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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