Update at the May 6, 2014 HIT Policy Committee meeting

If you are selling medical devices in the US, your devices are subject to new regulatory requirements under the FDA Unique Device Identification (UDI) rule. UL experts have…

Via Christi Women's Connection lecture on vitamins and supplements presented by Via Christi pharmacist Lyndsey Hogg, PharmD.

HHS New Media Webinar SeriesEpisode #2

Managing an FDA PreApproval Inspection

Preparing for an FDA PreApproval Inspection

A workshop on converting values to ethics in the industries regulated by the Food and Drug Administration.

The FDA enforces the Dietary Supplement Health and Education Act (DSHEA) law by inspecting dietary supplement manufacturers, packagers, labelers and holders for Current Good…