Article 23 Sep 2016 Time For A Reboot? FDA Issues Draft Guidance On When To Submit A 510(k) For A Software Change To An Existing Device United States Healthcare
Article 16 Sep 2016 FDA Finalizes Guidance On Low Risk General Wellness Devices United States Healthcare
Article 16 Sep 2016 FDA Proposes Important Revisions To Good Laboratory Practices Regulations United States Healthcare
