Dockets

Recently active federal rulemakings, soonest-closing first.

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Cardiac Ablation Catheters Generic Arrhythmia Indications UseFDANonrulemaking
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Channels of Trade Policy for Commodities with VinclozolinFDANonrulemaking
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Hospitals, Nursing Homes, Other Health Care FacilitiesFDANonrulemaking
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Evaluation of the Effects of Orally Inhaled & IntranasalFDANonrulemaking
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Exemptions from the Warning Label Requirement for Juice RequirementsFDANonrulemaking
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Submission to Food Additive Safety Office; Electronic Format, GeneFDANonrulemaking
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Joint Metal/Polymer Constrained Cemented or Uncemented ProsthesisFDANonrulemaking
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The Leaveraging Handbook, An Agency Resource for Effect CollaborationFDANonrulemaking
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Guidance ICH Q1D Bracketing & Matrixing Designs for StabilityFDANonrulemaking
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Available of Information Given to Advisory Committee MembersFDANonrulemaking
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Statistical Approaches Establishing BioequivalenceFDANonrulemaking
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Food Products Susceptible to Contamination with Allergenic ingredientsFDANonrulemaking
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Establishment & Operation of Clinical Trial Monitoring CommitteesFDANonrulemaking
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Pre-Store Leukocyte Reduction/Blood Components for TransfusionFDANonrulemaking
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Postmarketing Safety Reporting-Human Drug & Biological Products Including VaccinesFDANonrulemaking
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Patent Extension for Diphenylmethane Diisocyanate, 4,968,514FDANonrulemaking
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Poly(hexamethylenebiguanide)hydrochloride as a Preservative Food-ContactFDANonrulemaking
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Foodborne Pathogens in Raw-Frozen-Cooked-Partially CookedFDANonrulemaking
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Safe Use of Acidified Sodium Chlorite Solutions/Vegs & FruitsFDANonrulemaking
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Use of Mixture of Peroxyacetic Acid, Octanoic Acid, AceticFDANonrulemaking
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Corometrics Model 120 F-Series Maternal/Fetal Oxygen Saturization MonitoringFDANonrulemaking
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Premarket Approval for Medtronic AVE, Inc., Medtronic AVE BeStent 2 with Discrete Technology™FDANonrulemaking
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Veterinary Adverse Drug Reaction, Lack of Effect, ProductFDANonrulemaking
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Progress on Implementing for the Common Technical DocumentFDANonrulemaking
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Agency Information Collection Health & Diet SurveyFDANonrulemaking
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Medical Device Registration & ListingFDANonrulemaking
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Proposal to Debar Edwin Kokes; Notice of Opportunity for HearingFDANonrulemaking
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Withdrawal of 51 NDAs & 25 ANDAsFDANonrulemaking
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Regulation for Establishing Import TolerancesFDANonrulemaking
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Third-Party Submissions Review/Quality System InspectionsFDANonrulemaking
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Safety & Effectiveness of New Drug & Biological Products in Pediatric PatientsFDANonrulemaking
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Proposal to Debar Harry W. Snyder, Jr.; Opportunity for HearingFDANonrulemaking
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Safety or Effectiveness Not Reason for Withdrawal of ANDAFDANonrulemaking
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Assessment of Physician & Patient Attitudes Toward Direct-to-ConsumerFDANonrulemaking
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Proposal to Debar Renee Peugeot; Notice of Opportunity for HearingFDANonrulemaking
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Medical Devices: Third-Party Review Under FDAMA; Agency Information Collection ActivitiesFDANonrulemaking
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Rapid Response Surveys; Agency Information Collection ActivitiesFDANonrulemaking
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Electronic Interchange Standard for Digital ECG; Public MeetingFDANonrulemaking
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Institutional Review BoardsFDANonrulemaking
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Reports of Corrections & Removals: Agency Information Collection ActivitiesFDANonrulemaking
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Format & Content Requirements for OTC Drug Product LabelingFDANonrulemaking
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Prescription Drug User Fee ActFDANonrulemaking
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New Animal Drug Application, Form FDA 356 V, 21 CFR Part 514FDANonrulemaking
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Use of Opiate Analgesics in Various Patient PopulationFDANonrulemaking
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CGMP Regulations for Medicated FeedsFDANonrulemaking
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Preparation for ICH Meeting Tokyo, Japan, Common TechnicalFDANonrulemaking
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New Animal Drugs for Investigational; Agency Information Collection ActivitiesFDANonrulemaking
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Substances Prohibited from Use in Animal Food/Feed RuminantFDANonrulemaking
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Rescind Approval of Solid Oral Dosage Form of MetaxaloneFDANonrulemaking
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Definition for the Term 'Stone Ground' for Wheat FlourFDANonrulemaking
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