Article 03 Nov 2021 FDA's Long-Awaited De Novo Classification Rule Is Finally Here United States Healthcare
Article 26 Jan 2018 Moratorium On Medical Device Excise Tax Extended For Two Years United States Healthcare
Article 25 Jan 2018 What Pharma Companies Need To Know About FDA's New Draft IVD Guidance United States Healthcare
Article 21 Aug 2017 FDA Announces Digital Health Innovation Action Plan To Implement 21st Century Cures Act United States Healthcare
Article 09 Jun 2017 California Bill May Upend Pharma Company Interaction With HCPs United States Healthcare
Article 10 May 2017 OCR Announces First HIPAA Settlement With Wireless Health Services Provider United States Healthcare
Article 27 Feb 2017 FDA Devices Center Issues Multiple Guidances In The Obama Administration's Final Months United States Healthcare
Article 15 Dec 2016 21st Century Cures Act And Medical Device Regulatory Pathways United States Healthcare
Article 17 Nov 2016 Top Takeaways From FDA Draft Guidance On Software As A Medical Device United States Healthcare
Article 10 Oct 2016 10 Key Takeaways From FDA's Draft Guidance On 510(K) Modifications United States Healthcare
Article 06 Sep 2016 FDA Uses Summer To Issue Numerous Device Guidance Documents United States Healthcare
Article 08 Feb 2016 FDA Issues New Draft Guidance On Postmarket Cybersecurity For Medical Devices United States Healthcare
Article 05 Nov 2014 Medical Device Update: Distinguishing Medical Device Recalls From Medical Device Enhancements United States Healthcare
Article 03 Sep 2014 Medical Device Update: FDA Issues Draft Guidance On Streamlined De Novo Classification Process United States Healthcare
Article 11 Aug 2014 FDA Issues Final Guidance On 510(k) Determinations, Use Of "Split" Predicates Strongly Discouraged United States Healthcare