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Advertising & Promotion

  • Dec 19, 2018
    ABPI Revises Code of Practice
  • Dec 19, 2018
    San Francisco Sues Opioid Makers Over Sales Practices
  • Dec 17, 2018
    WLF Calls on CMS To Withdraw Proposed Rule Mandating Price Disclosure in Drug DTC TV Ads
  • Dec 14, 2018
    KOLs Find Reasons for Negative Results
  • Dec 14, 2018
    NAD Recommends Two Supplement Makers Discontinue Sun Protection Claims
  • Dec 14, 2018
    NAD Refers Laser Device Claims to FTC, FDA
  • Dec 13, 2018
    Alaskan Natives Sue Companies Over Marketing of Opioid Products
  • Dec 13, 2018
    Four Ad Promotion Questions for 2019
  • Dec 13, 2018
    Senator Asks Pfizer for Marketing Costs
  • Dec 11, 2018
    IFPMA Revises Code of Practice, Bans Gifts
  • More

Good Clinical Practice

  • Feb 24, 2019
    Germany Finds Some 1,300 Trials May Be Affected by Brexit
  • Feb 22, 2019
    FDA Provides Resources for Final Rule on Acceptance of Device Trial Data
  • Feb 22, 2019
    FDA Issues Draft Guidance on Trial Design Issues for Nicotine Replacement Therapy Products
  • Feb 21, 2019
    Study Finds Structural and Clinical Barriers to Cancer Trial Participation
  • Feb 20, 2019
    FDA Issues Guidance on Investigational Tobacco Product Studies
  • Feb 19, 2019
    Researchers Call for Research Policy Board
  • Feb 13, 2019
    Florida Senate Considers Right-to-Try Bill for Investigational Stem Cell Treatments
  • Feb 12, 2019
    Idaho Bill Mandates Insurance Coverage for Routine Patient Care in Clinical Trials
  • Feb 12, 2019
    HHS OIG Reviewing 12 NIH Research Cases
  • Feb 12, 2019
    FDA-CTTI Set Workshop on Patient Perspectives on Clinical Trials
  • More

U.S. Food Labeling

  • Jul 21,2015
    Senate Bill Sets One-Year Moratorium on Menu Labeling, Mandates Labels for GMO Salmon
  • Jul 20,2015
    Three Convicted in PCA Salmonella Outbreak To Be Sentenced Sept. 21
  • Jul 20,2015
    FSIS Preparing To Crack Down On Meats Without Nutrition Labels
  • Jul 16,2015
    GMO Preemption Bill Clears House Agriculture Committee
  • Jul 9,2015
    White House Memo Orders Agencies That Police GMOs to Coordinate More
  • Jul 9,2015
    FDA Grants Chains One More Year To Implement Menu Labeling Changes
  • Jun 19,2015
    U.S. Delays Sanctions Over COOL Via Arbitration Request to WTO
  • Jun 16,2015
    Industry Has Three Years To Phase Out Trans Fats, Change Labels
  • Jun 12,2015
    House Passes Bill Gutting COOL Rules
  • Jun 12,2015
    Labeling Considerations Factor Into Food Importation Program
  • More

FDA Regulation & Enforcement

  • Apr 29, 2022
    OPDP Researchers Will Conduct Tradeoff Analysis of Product Claims Made to Consumers and Physicians
  • Apr 18, 2022
    Marketers Sentenced for Roles in Compounded Drug Kickback Scheme Through Oklahoma Pharmacy
  • Apr 18, 2022
    Survey Finds ‘Organic’ Unclear to Consumers; Antibiotics Found in Cattle Labeled ‘RWA’
  • Apr 18, 2022
    District Court Dismisses Case Against Merck over Vaccine Marketing
  • Apr 18, 2022
    Members of Congress Question McKinsey & Co.’s Simultaneous Work for FDA and Opioid Companies
  • Apr 14, 2022
    FDA Upholds Position That NAC Is Not a Supplement, Promises Enforcement Guidance
  • Apr 13, 2022
    FDA Asks Congress for New Enforcement Powers: Will Remote Regulatory Assessments Become Mandatory?
  • Apr 13, 2022
    OPDP Issues Untitled Letter Over DTC Video, Efficacy Webpage
  • Apr 7, 2022
    Fifth Circuit Affirms Dismissal of Louisiana Tort Law Claims Brought Against ICD Manufacturer
  • Apr 6, 2022
    Former Pharma CEO Charged with Conspiracy To Defraud the FDA, Distribution of Contaminated Drugs
  • More

Medical Devices

  • Apr 17, 2018
    FDA: Two New Guidance Documents Should Help Spur Development of NGS-Based In Vitro Diagnostics
  • Apr 11, 2018
    New 510(k) Pathway Will Allow Use of Performance Criteria To Demonstrate Substantial Equivalence
  • Apr 5, 2018
    Federal District Court Dismisses Nearly All of Patient’s Florida Law Claims Against Breast Implant Maker
  • Mar 28, 2018
    Alere Resolves False Claims Act Allegations Based on Triage Test Devices’ ‘Unreliable’ Results
  • Mar 21, 2018
    Draft Guidance on December 2016 Combination Products Postmarketing Safety Reporting Final Rule Released
  • Mar 14, 2018
    Heart Pump Manufacturer Agrees To Pay $3.1 Million To Resolve False Claims Allegations Concerning ‘Lavish’ Physician Meals
  • Mar 12, 2018
    CDRH: Duodenoscope Makers Are Not Complying with October 2015 Postmarket Surveillance Orders
  • Mar 7, 2018
    Tackling Issue of ‘Component Preemption,’ Third Circuit Dismisses Some Tort Claims Against Device Maker
  • Mar 1, 2018
    Federal District Court Dismisses Patient’s Failure-To-Warn Claim Against ICD Lead Manufacturer
  • Feb 23, 2018
    FDA Issues Final Rule on Acceptance of Device Trial Data
  • More

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