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ASC Circular 2018-003 – Rendition of GENERIC NAMES per AO 2016-008 (Revised Rules and Regulations Governing the Generic Labeling Requirements of Drug Products for Human Use)

The Center for Drug Regulation and Research (CDRR) of the Food and Drug Administration (FDA) has called the attention of the Ad Standards Council (ASC) on the proper rendition of the GENERIC NAME given the various forms of media. In connection with this, please find below basic guidelines by medium per AO 2016-0008 – Revised […]

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