Article 14 Mar 2022 FDA Issues Guidance To Clarify Recommendations Regarding Timely Initiation Of Voluntary Recalls United States Healthcare
Article 30 Dec 2021 FDA Issues Draft Guidance To Clarify Referencing Of The Terms "Device" And "Counterfeit Device" United States Healthcare
Article 13 Dec 2021 FDLI's Enforcement, Litigation, And Compliance Conference: For The Drug, Device, Food, And Tobacco Industries United States Healthcare
Article 15 Jul 2021 FDA Publishes Guidance On The Enhanced System Under The DSCSA Going Into Effect On November 27, 2023 United States Healthcare
Article 05 Jul 2021 FDA Interprets Terms Used In Definitions Of Suspect And Illegitimate Product Under The DSCSA United States Healthcare
Article 25 Jun 2021 FDA Publishes Guidance On The Identification And Notification Of Suspect Products As Part Of The Implementation Of The Drug Supply Chain Security Act United States Healthcare
Article 23 Jun 2021 DOJ Announces $22 Million False Claims Act Settlement With The University Of Miami For Provider-Based Rule Violations Involving Laboratory Tests United States Government
Article 31 May 2021 FDA Publishes Guidance On Remote Interactive Evaluations For Oversight Of Drug Manufacturing And Bioresearch Monitoring Facilities During The COVID-19 Public Health Emergency United States Healthcare
Article 24 May 2021 FDA Conforms Regulations To Exclude Certain Software Functions From The Definition Of Device United States Healthcare