1. Medical product communications that are consistent with the FDA-required labeling: questions and answers Publication: Silver Spring, MD : Center for Drug Evaluation and Research, June 2018 Subject(s): CommunicationDrug Labeling -- standardsProduct Labeling -- standardsEquipment and Supplies -- standardsPharmaceutical Preparations -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
2. Extension of certain tobacco product compliance deadlines related to the final deeming rule: (revised) Publication: Silver Spring, MD : Center for Drug Evaluation and Research, August 2018 Subject(s): Product Labeling -- standardsTobacco Products -- standardsTobacco Industry -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
3. Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff Publication: Silver Spring, MD : Center for Biologics Evaluation and Research, January 16, 2018 Subject(s): Equipment and Supplies -- classificationProduct Labeling -- standardsProduct Packaging -- standardsHumansUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
