FDA classifies simple in vitro diagnostic devices for detecting Bacillus species secreted proteins in human clinical samples as Class II medical devices with special controls.
Center for Scientific Review will hold closed meetings to review and discuss NIH grant applications and related administrative matters on specified dates.
Federal agency forms are undergoing Paperwork Reduction Act review to assess burden on small businesses and other respondents.
Federal agencies are reviewing multiple forms under the Paperwork Reduction Act to reduce burden on small businesses and other respondents.
CDC seeks public comment on the Public Health Emergency Management Tool data collection under the Paperwork Reduction Act of 1995 to assess emergency management capacity in partner countries.
Federal agencies are reviewing multiple forms for paperwork reduction compliance under the Paperwork Reduction Act; public comment period open for burden reduction assessments.
FDA withdraws approval of SpecGx LLC's abbreviated new drug application for Methylphenidate Hydrochloride Extended-Release tablets in 27mg, 36mg, and 54mg strengths per the applicant's request.
The FDA renews its Science Board advisory committee for an additional two years, with the new charter expiring June 26, 2028.
FDA requests OMB clearance for information collection activities related to Current Good Manufacturing Practice regulations for Type A medicated articles and medicated feeds under the Paperwork Reduction Act of 1995.
FDA submission to OMB for Paperwork Reduction Act review of information collection requirements for dietary supplement manufacturing, packaging, labeling, and holding operations.
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