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

  • Jul 16, 2016
    ERSP Recommends Marketer Modify or Discontinue Some Claims for Laser Therapy Hair Cap
  • Jul 14, 2016
    District Court Allows False Advertising Case To Move Forward
  • Jul 11, 2016
    Analysis of DTC Banner Ads Finds Companies Need More Guidance
  • Jul 11, 2016
    Departure of HHS Chief Counsel Could Affect FDA Marketing Policies
  • Jul 11, 2016
    Pfizer Agrees To Standards for Marketing Opioids
  • Jul 8, 2016
    Astellas UK Suspended from ABPI for Advisory Board Meeting Deemed Too Promotional
  • Jul 5, 2016
    U.S. Appeals Court Reinstates ‘False Advertising’ Claims Against Dietary Supplement Maker
  • Jul 5, 2016
    District Court Dismisses RICO Complaint Against Abbott over Off-label Promotion of Depakote
  • Jun 20, 2016
    Study Finds Meals May Increase Prescribing Rates
  • Jun 20, 2016
    Focus Labs Warned for False and Misleading Labeling on Medical Food
  • More

Good Clinical Practice

  • Mar 22, 2017
    Kentucky Gov. Signs Right-to-Try Law
  • Mar 17, 2017
    Group’s Transparency Proposals for FDA Include Release of Trial Data
  • Mar 16, 2017
    Health Canada Releases Paper on Proposed Approach To Public Release of Trial Data
  • Mar 16, 2017
    NEMJ Article Details Patient-Funded ‘Study’ That Resulted in Patient Injury
  • Mar 16, 2017
    Kentucky Right-to-Try Bill Sent to Governor
  • Mar 15, 2017
    Iowa Senate Approves Right-to-Try Bill
  • Mar 14, 2017
    Analysis of Pediatric Trial Finds Fewer Minority Parents Approached for Consent
  • Mar 12, 2017
    Gottlieb Nominated To Head FDA as Commissioner of Food and Drugs
  • Mar 10, 2017
    TransCelerate Outlines 2017 Plans
  • Mar 9, 2017
    Wisconsin Assembly OKs Right-to-Try Bill
  • More

FDA Regulation & Enforcement

  • Aug 7, 2019
    DeLauro Reintroduces DTC Drug Ad Bill
  • Aug 7, 2019
    Review of Patient Assistance Programs Finds They Might Bolster Expensive Drugs
  • Aug 6, 2019
    Analysis Finds Half of NCI Center Directors Received Industry Payments
  • Aug 6, 2019
    House Committee Leaders Signal Concerns Over Stem Cell Therapies, FDA’s Work To Ensure Compliance
  • Aug 5, 2019
    Groups Support Challenge to Arkansas ‘Veggie’ Labeling Law
  • Aug 2, 2019
    Arizona Files Opioids Case With U.S. Supreme Court
  • Aug 1, 2019
    Alleged Lack of Risk Info Cited in Untitled Letter for DTC TV Ad
  • Jul 31, 2019
    FSIS Rejects Request to Require New Warning on Processed Meat, Poultry Labels
  • Jul 31, 2019
    FDA, HHS Propose Two Possible Pathways for Importing Prescription Drugs into the United States
  • Jul 25, 2019
    DOJ: Spinal Device Manufacturer, Two Company Officials Paid Surgeons Millions in Illegal Kickbacks
  • More

Medical Devices

  • Apr 30, 2012
    Final Guidance on Benefit-Risk Determinations for PMA, De Novo Devices Released by CDRH, CBER
  • Apr 30, 2012
    FDA SOP for Response to Cargo Thefts Outlines Agency's Role in Crafting Public Notifications
  • Apr 30, 2012
    Pilot Program Can Help Medical Device Companies Avoid Routine Quality Systems Inspections by FDA
  • Apr 30, 2012
    GAO: Device Review Times Increasing Despite FDA Success in Meeting Performance Goals
  • Apr 30, 2012
    Guidances Outline Procedures, User Fees for Classification Information Requests
  • Mar 31, 2012
    FDA Will Survey Providers About Device Labeling
  • Mar 31, 2012
    IRS Releases Proposed Regulations for Device Tax
  • Mar 31, 2012
    New Draft Guidance Outlines Use of Study Data Standards for Submissions in Electronic Format
  • Mar 31, 2012
    FDA Asks Denture Adhesive Makers For Help Addressing Adverse Events
  • Mar 31, 2012
    Medtronic Says DOJ Ends Probe Into Biliary Stent Marketing
  • 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.