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Barnes & Thornburg
Lynn Tyler
Lynn Tyler
Barnes & Thornburg
FDA Issues Final Guidance On Postmarket Management Of Cybersecurity In Medical Devices
14 Mar 2017 | United States
FDA Issues Draft Guidance On Voluntary Labeling Of GMO Foods
09 Dec 2015 | United States
FDA Publishes Final Rule On Foreign Supplier Verification Program
25 Nov 2015 | United States
FDA Issues Final Produce Safety Rule
24 Nov 2015 | United States
FDA Publishes Final Rule On Accreditation Of Third-Party Certification Bodies To Conduct Food Safety Audits
24 Nov 2015 | United States
Will FDA Finally (And Officially) Define "Natural?"
24 Nov 2015 | United States
Food, Drug And Device Law Alert - FDA Publishes Final Rule On Preventive Controls For Human Food
29 Sep 2015 | United States
Federal Court Authorizes Pharmaceutical Firm To Engage In Off-label Promotion Using Certain Specific Information And Statements
18 Aug 2015 | United States
FDA Issues Proposed Rule And Draft Guidance On User Fee Program For Accreditation Of Third-Party Auditors/Certification Bodies To Conduct Food Safety Audits And To Issue Certifications
29 Jul 2015 | United States
FDA Issues Proposed Rule On Disclosing Added Sugars On Nutrition Facts Label
29 Jul 2015 | United States
FDA Issues Draft Guidance On Direct Marking Of UDI On Devices
10 Jul 2015 | United States
FDA Issues Draft Guidance On Factors To Consider When Making Benefit-Risk Determinations For IDEs
25 Jun 2015 | United States
FDA Issues Draft Guidance On Voluntary Qualified Importer Program Under The Food Safety Modernization Act
09 Jun 2015 | United States
FDA Issues Draft Guidance On Mandatory Food Recalls Under The Food Safety Modernization Act
28 May 2015 | United States
FDA Issues Draft Guidance On Use Of Patient Preference Information In Certain Medical Device Pre-Market Submissions And Labeling
28 May 2015 | United States
FDA Releases Draft Guidance On Using Clinical Data From Studies Conducted Outside The United States To Support Approval Of Medical Devices
12 May 2015 | United States
FDA Releases Final Guidance On Expedited Access Program For Medical Devices
22 Apr 2015 | United States
FDA Proposes To Amend Regulations On Food Facility Registration
21 Apr 2015 | United States
FDA Issues Final Guidance On Reprocessing Medical Devices
10 Apr 2015 | United States
FDA Issues Final Guidance Documents On Medical Device Data Systems And Medical Mobile Apps
26 Feb 2015 | United States
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