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 12, 2016
    Washington Bill Requires Drug Makers To Report Costs of High-priced Drugs
  • Feb 11, 2016
    Joint Paper Calls for Feds To Allow Pre-market Communication with Insurance Companies
  • Feb 10, 2016
    Maryland Bills Seek Disclosure of Industry Financial Arrangements
  • Feb 8, 2016
    FTC, Maine AG Settle Weight-Loss Supplement Case
  • Feb 3, 2016
    New York Senate Resurrects Bill Requiring Marketing Reporting, Eliminating Ad Deduction
  • Feb 2, 2016
    FDA Needs To Address Amarin Off-label Issues or Lose Its Authority: Internal Medicine Viewpoint
  • Jan 27, 2016
    Study Examines Characteristics of Marketing Trials
  • Jan 26, 2016
    Survey Finds Doctors Prefer Direct Touch
  • Jan 23, 2016
    CDER Plans To Release Four Advertising Related Draft Guidances in 2016
  • Jan 21, 2016
    First 2016 OPDP Untitled Letter Concerns YouTube Video
  • More

Good Clinical Practice

  • Dec 15, 2016
    FDA, OHRP Issue Joint Electronic Informed Consent Guidance
  • Dec 14, 2016
    OHRP 2017 International Human Research Standards Compilation Adds Six Nations
  • Dec 7, 2016
    Ohio Senate Approves ‘Right-to-Try’ Bill
  • Dec 7, 2016
    CIOMS Revises Ethical Research Guidelines
  • Dec 5, 2016
    ABPI Finds Trial Result Disclosure for Approved Drugs Remains Steady in Europe
  • Dec 5, 2016
    Researchers Find Patients Normally Excluded from Cancer Trials Respond Well
  • Dec 5, 2016
    Group Looks To Optimize Exploratory Trials
  • Dec 2, 2016
    Partnership Examines Cancer Trial Eligibility Criteria
  • Dec 2, 2016
    Cures Bill Allows Consent Waiver for FDA Trials, Single IRB for Devices
  • Dec 2, 2016
    EMA Analysis Finds Early Trial Design Can Aid Ultimate Development Success
  • More

FDA Regulation & Enforcement

  • Jun 5, 2019
    OPDP Issues Second Untitled Letter for 2019
  • Jun 4, 2019
    Major Statement Rule Pushed to 2020
  • Jun 4, 2019
    Almirall Pays Feds, California $6.6 Million To Resolve Kickback Allegations
  • Jun 4, 2019
    Three More States, D.C. Sue Purdue Pharma
  • May 29, 2019
    Court: State Law Tort Claims Related to Knee Implant Device Approved Through PMA Are Preempted
  • May 29, 2019
    FDA Is Closer to Regulating ‘Healthy,’ While ‘Natural’ Continues to Play Out in Court
  • May 28, 2019
    New DOJ Corporate Compliance Program Guidance Shows How Prosecutors Scrutinize Companies’ Compliance Efforts
  • May 23, 2019
    Supreme Court: Impossibility Preemption in Failure-To-Warn Cases Raises Question for a Judge, Not a Jury
  • May 23, 2019
    Draft Guidance Would Allow Alternative Name for Potassium Chloride
  • May 20, 2019
    Jury Finds for Allergan in False Advertising Case
  • More

Medical Devices

  • Jun 30, 2011
    FDA Makes Enforcement, Compliance Histories Public
  • Jun 30, 2011
    $3.4 Billion in Health Care Fraud-related Recoveries Expected in Just First Half of FY 2011, OIG Says
  • Jun 30, 2011
    ReGen Biologics Sues FDA for Rescinding Clearance of Its Menaflex Collagen Scaffold
  • Jun 30, 2011
    FDA, CMS Reviewing Regs To Eliminate Duplication
  • Jun 30, 2011
    CAPA Leads Warning Letter Citations, FDA Says
  • Jun 30, 2011
    FDA Keeping Eye on Products From Japan
  • May 31, 2011
    STERIS Corp. Working With FDA To Review, Revise Promotional Materials for Certain Sterilization Devices
  • May 31, 2011
    Outreach Has Its Drawbacks, Ombudsman Says
  • May 31, 2011
    Postmarket Reforms Likely As Part of MDUFMA III
  • May 31, 2011
    Industry Not Yet Sold on Database of Labeling, Photos
  • 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.