All News | FDA

Advertising & Promotion

Mar 29, 2017
McCaskill Investigates Marketing Practices of Opioid Manufacturers
Mar 28, 2017
NY AG Settles with Three App Makers Over Marketing and Privacy Practices
Mar 24, 2017
Study of ‘Low T’ DTC Ads Finds Ads Did Their Job Maybe Too Well
Mar 21, 2017
Chicago Releases Proposed Rules for Drug Sales Rep Licensing; Comments Due April 12
Mar 20, 2017
FDA Delays ‘Intended Uses’ Rule for Year, Seeks Comment on Four Questions
Mar 20, 2017
Importance of Recent Draft Guidances Is Getting Lost in the Transition of Administrations
Mar 17, 2017
FTC Settles with Florida Operation Over Email Marketing, Weight-loss Claims and Endorsements
Mar 16, 2017
DTC Marketing Needs to Consider Price
Mar 15, 2017
Consent Decree Shuts Down Dietary Supplement Maker; FDA Had Issued No Warning Letter
Mar 15, 2017
Iowa AG Sues Companies Over Water Claims

Good Clinical Practice

Oct 5, 2017
Cancer Groups Call for Broader Eligibility Criteria
Oct 5, 2017
OPDP Study Finds Little Physician Understanding of Clinical Trial Terms
Oct 3, 2017
FDA Allows Single IRB Reviewer To Approve Expanded Access Requests
Oct 3, 2017
Analysis Finds Minorities and Elderly Underrepresented in Cancer Trials
Oct 2, 2017
Four European Groups Release Paper on Trials for Therapies Using Genetically Modified Organisms
Oct 2, 2017
CDRH Issues Final Guidance Detailing Study Designs for HPV IVD Trials
Oct 1, 2017
Survey Examines E-Clinical Data Landscape
Sep 25, 2017
FDA-OHRP Release Joint Guidance on IRB Minutes
Sep 22, 2017
Randomized Trial Finds Education Can Reduce Therapeutic Misconception
Sep 22, 2017
FDA Plans Oct. 27 Workshop on Drug Development for Pediatric Heart Failure

U.S. Food Labeling

Jul 31,2011
FSIS Proposes Rule on Labeling Raw Meat and Poultry Products Containing Added Solutions
Jul 31,2011
FDA Asked To Create National Nutrition Database
Jul 31,2011
Class Action Suit in U.S. Court Targets Dreyer's 'All Natural' Ice Cream Labeling
Jul 31,2011
Food Industry Releases Own Set of Nutrition Criteria for Advertising to Children
Jul 31,2011
U.S. Drops Opposition to Voluntary Labeling of Biotech Foods at Codex Alimentarius
Jul 31,2011
Product Recalls
Jul 31,2011
FSIS Denies AMI Petition on Irradiation Labeling
Jul 31,2011
FSIS Issues Notice to Inspectors on Undeclared Allergens in Meat and Poultry Products
Jun 30,2011
FDA Provides Qualified Health Claims for Certain Milk-based Infant Formula Products
Jun 30,2011
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FDA Regulation & Enforcement

Feb 27, 2020
FTC Files Action Against Two Firms Alleging False Product Claims
Feb 26, 2020
Coronavirus Outbreak Forces FDA To Suspend Inspections in China; Agency Will Use Other Monitoring Tools
Feb 25, 2020
FDA Accuses Jimmy John’s of Selling Contaminated Food, Citing ‘Multiple’ Outbreaks Over Seven Years
Feb 24, 2020
FTC Seeks Public Comment on Endorsement and Testimonial Guides
Feb 20, 2020
Seventh Circuit: Design Defect Claim Involving Ethicon’s Transvaginal Mesh Device Is Not Preempted
Feb 19, 2020
Animal Rx Drug Distributor To Pay More Than $52 Million To Resolve Misbranding Allegation
Feb 18, 2020
Bill Introduced in House Requiring List Prices in Drug DTC Ads
Feb 12, 2020
OIG Advisory Opinion Clears Drug Maker’s Patient Travel Expense Program from Antikickback Sanctions
Feb 12, 2020
Class Action Against Coca-Cola Co. Challenges ‘Just a Tad Sweet’ Claim
Feb 12, 2020
Small Firm Nutrition Facts Compliance Guide Now Available

Medical Devices

Apr 1, 2014
CDRH SOP on Communicating Changes in Center’s Expectations for Data in Submissions Finalized
Mar 27, 2014
Proposed Rule Revises Classification Procedures, Identifies Five Categories of Devices for Class III
Mar 18, 2014
AdvaMed Says Device Tax Is Costing Jobs, R&D
Mar 18, 2014
FDA Updates HDE Guidance To Reflect FDASIA Changes
Mar 17, 2014
FDA Updates HDE Guidance To Reflect FDASIA Changes; ADN Definition Amended, Terms Clarified
Mar 14, 2014
Warning Letter Blasts Device Maker for Web Claims
Mar 14, 2014
ICCBBA Becomes Third UDI Issuing Agency
Mar 13, 2014
Updated Guidance Addresses FDA’s Processes for IVD Test Categorization Under CLIA, Waiver Procedure
Mar 13, 2014
Final Guidance on Pre-Submission Program, Meetings With FDA Staff Released
Mar 10, 2014
Average Clearance Time for 510(k)s Was 166 Days in 2013; No Effect Yet From Refuse-To-Accept Policy

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