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Federal Register|June 3, 2015
Medical devices; immunology and microbiology devices; classification of multiplex nucleic acid assay for identification of microorganisms and resistance markers from positive blood cultures. Final order
Federal Register|July 10, 2015
Revocation of General Safety Test Regulations That Are Duplicative of Requirements in Biologics License Applications. Final rule
Federal Register|June 23, 2017
Erratum: Findings of Research Misconduct; Correction
Federal Register|August 7, 2023
Erratum: Findings of Research Misconduct; Correction
Federal Register|January 2, 2003
Cold, cough, allergy, bronchodilator, and antiasthmatic drug products for over-the-counter human use; final monograph for combination drug products. Final rule
Federal Register|November 7, 2002
Poison prevention packaging requirements; exemption of hormone replacement therapy products. Final rule
Federal Register|December 12, 2002
Labeling of diphenhydramine-containing drug products for over-the-counter human use. Final rule
Federal Register|May 11, 2002
Status of certain additional over-the-counter drug category II and III active ingredients. Final rule
Federal Register|May 22, 2002
Tribal Self-Governance Amendments of 2000. Final rule
Federal Register|June 7, 2002
New drug and biological drug products; evidence needed to demonstrate effectiveness of new drugs when human efficacy studies are not ethical or feasible. Final rule
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