Skip to main content
Home
FDA
  • LOG IN
  • Thompson FDA
  • Manage Account
  •  
  • 1.800.677.3789

Main navigation

  • LIBRARY
    • FDA Enforcement Manual
    • Guide to Good Clinical Practice
    • FDA Advertising and Promotion Manual
    • Guide to Medical Device Regulation
    • Guide to U.S. Food Labeling Law
  • MY RESEARCH
  • NEWS
    • All News
    • FDA Intelligence
  • DATABASES
    • FDA Enforcement Database
    • Clinlaw State Database
  • RESOURCES
    • FDA Forms
    • Special Reports
    • Judicial Opinions
    • Interactive Tools
  • AGENCY GUIDANCE
    • Enforcement Guidance
    • Clinical Trials Guidance
    • Advertising and Promotion Guidance
    • Medical Device Guidance
    • Food Labeling Guidance
  • ASK THE EXPERT

Login to the Thompson
FDA Compliance Expert

Enter your FDA username.
Enter the password that accompanies your username.
Forgot password?

Questions? Give us a call! 1-800-677-3789

Advertising & Promotion

  • Feb 23, 2018
    Philadelphia Sues Opioid Makers Under Pa. Unfair Practices, Consumer Protection Laws
  • Feb 22, 2018
    Anti-aging Supplement Maker Settles with FTC
  • Feb 22, 2018
    OPDP’s First Untitled Letter of 2018 Hits Opioid Manufacturer’s Exhibit Booth for Minimizing Risks
  • Feb 20, 2018
    Senate Bill Requires Controlled Substance TV Ad Review Prior To Airing
  • Feb 17, 2018
    Ky. Supreme Court Allows Drug Advertising Case To Continue
  • Feb 14, 2018
    Senate Report Details Pain Advocacy Groups’ Financial Connection to Opioid Manufacturers
  • Feb 13, 2018
    U.S. Files Complaint Against Supply Company Alleging Kickbacks To Physicians
  • Feb 13, 2018
    Purdue Stops Marketing Opioids to Prescribers
  • Feb 9, 2018
    Bill Requiring Cost Reporting Introduced in Oregon
  • Feb 8, 2018
    Alabama Sues Purdue Over Opioid Marketing
  • More

Good Clinical Practice

  • Jun 23, 2018
    Questions Abound Over Returning Individual Research Results
  • Jun 23, 2018
    FDA Sets Public Docket on Data Standards
  • Jun 22, 2018
    OCR Releases HIPAA Guidance Mandated by Cures Act
  • Jun 22, 2018
    Recommendations Developed for Expanding Lung Cancer Trial Eligibility Criteria
  • Jun 21, 2018
    ClinicalTrials.gov Details Issues To Consider in Using Database
  • Jun 20, 2018
    Revised Draft Guidance on Humanitarian Device Exemptions Incorporates Changes Under Cures Act, FDARA
  • Jun 19, 2018
    Revised Common Rule Implementation Pushed Back to January 2019
  • Jun 18, 2018
    Group Calls for Alzheimer’s Research To More Fully Examine Sex and Gender Differences
  • Jun 16, 2018
    NIH To End Controversial Alcohol Study
  • Jun 16, 2018
    ACRP to Develop CRC Hiring Guidelines
  • More

U.S. Food Labeling

  • Jun 14,2013
    Maine’s House Passes GMO Labeling Bill, Senate Committee Clears Bill for Floor Vote
  • Jun 12,2013
    FSIS Issues Long-overdue Proposal for Mechanically Tenderized Beef, Guidance for Cooking Instruction
  • Jun 7,2013
    Connecticut Passes Modified GMO Labeling Bill, Governor Pledges To Sign the Legislation
  • May 31,2013
    Connecticut House Passes GMO Labeling Measure, Implementation Differs Sharply From Senate Version
  • May 31,2013
    Warning Letter Blasts Supplement Labeling Claims
  • May 31,2013
    Letter Blasts Supplement Maker for Medical Food-like Claims
  • May 29,2013
    Senate Push To Protect State GMO Labeling Efforts Fails in Procedural Vote
  • May 28,2013
    AMS Finalizes COOL Changes, Revises Labeling Standards for Muscle-Cut Meats
  • May 22,2013
    Connecticut and Vermont Move Closer To Passing Legislation Mandating GMO Labeling Disclosure
  • May 20,2013
    GMO Advocacy Group Blasts Farm Bill Rider as Effort To Quash GMO Labeling
  • More

FDA Regulation & Enforcement

  • Apr 1, 2021
    Consumer Groups Want FDA To Act Quickly Against ‘Fortified’ Beer
  • Mar 31, 2021
    Free Drug Program Would Not Lead to Sanctions, HHS OIG Concludes in First Advisory Opinion of 2021
  • Mar 31, 2021
    Boston Scientific Settles with States Over Marketing of Surgical Mesh Devices
  • Mar 25, 2021
    N.Y. Dietary Supplement Firm Is Shut Down After Court Modifies DOJ’s Proposed Injunction Order
  • Mar 24, 2021
    Court Declines To Dismiss on Preemption Grounds State Law Claims Involving a PMA Cardiac Device
  • Mar 24, 2021
    Fresenius Kabi Oncology Sentenced To Pay $50 Million for Concealing, Destroying Records Before FDA Inspection
  • Mar 21, 2021
    OPDP Researchers Move Ahead with Proprietary Name Study
  • Mar 17, 2021
    Criminal Charges Brought Against Supplement Firm and its Operator for Allegedly Refusing FDA Inspections
  • Mar 17, 2021
    Senate Unanimously Passes Bill To Add Sesame to List of Major Allergens
  • Mar 15, 2021
    OPDP Issues First Untitled Letter of 2021
  • More

Medical Devices

  • Mar 10, 2016
    Call for Comments on Refurbishing, Reconditioning Devices May Signal Additional FDA Scrutiny
  • Mar 4, 2016
    FDA Extends Comment Period for Interoperable Devices Draft Guidance
  • Mar 3, 2016
    Olympus $646 Million Settlement Includes Largest Anti-Kickback Penalty Ever Paid by Device Company
  • Mar 2, 2016
    Report Urges Manufacturers To Follow Recommendations in FDA’s Draft Guidance on Device Cybersecurity
  • Feb 29, 2016
    FDA Solicits Input To Create National Evaluation System That Will Harness ‘Real-World’ Device Data
  • Feb 25, 2016
    CDRH Seeks Coverage Organizations Interested in Attending Device Pre-Submission Meetings
  • Feb 24, 2016
    Dr. Robert M. Califf Confirmed by Senate as New Commissioner of Food and Drugs
  • Feb 21, 2016
    BIO’s Scott Whitaker Chosen as New President, CEO at AdvaMed
  • Feb 19, 2016
    Patel Blog Post on Device Interoperability Stresses Patient Safety
  • Feb 18, 2016
    FDA Proposes Delay in Enforcing Deadlines for Removing Some Non-UDI Coding from Devices
  • More

THOMPSON FDA

  • Thompson FDA
  • About Us
  • Manage Account
  • Our Parent Company

COMPLIANCE EXPERT

  • News
  • My Research
  • Our Experts
  •  

RESOURCES

  • FDA Forms
  • Special Reports

HELP

  • Customer Support
  •  
  •  
  •  
  •  

CONTACT

  • headquarter Headquarters
  • contact-number 1.800.677.3789
  • Contact Us
  •  

Copyright © Thompson FDA, a division of CBIS. All rights reserved.

  • Terms
  • Privacy

FDA NEWS
YOU CAN USE

Get instant, free access to the latest news and analysis to keep up with the shifting requirements, recommendations, and expectations of the FDA.

Something went wrong. Please try after some time.