Article 16 Oct 2019 Is Your Software A Medical Device? FDA Issues Six Digital Health Guidance Documents United States Healthcare
Article 29 Aug 2019 Reviewing Key Principles From FDA's Artificial Intelligence White Paper United States Healthcare
Article 26 Jul 2019 FDA's Breakthrough Device Program: Opportunities And Challenges For Device Developers United States Healthcare
Article 18 Jan 2017 21st Century Cures: Food And Drug Administration (FDA) Drug Provisions United States Healthcare
Article 02 Nov 2016 CMS, FDA Parallel Review Program For Medical Devices Extended Indefinitely United States Healthcare
Article 17 Oct 2016 FDA Proposes To Modify Good Laboratory Practice Regulations, Broaden Application And Authority United States Healthcare
Article 10 Oct 2016 FDA Finalizes Rule Governing Establishment Registration And Listing For Human Drugs United States Healthcare
Article 03 Oct 2016 FDA Issues Draft Guidance On Risk Evaluation And Mitigation Strategy (REMS) Determinations United States Healthcare
Article 22 Sep 2016 FDA Extends Deadline For Removal Of NDC And NHRIC Numbers From Device Labeling And Packaging United States Healthcare
Article 21 Sep 2016 FDA Announces Public Hearing On Off-Label Communications; Registration Deadline October 19, 2016 United States Healthcare