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Advertising & Promotion

  • Jan 30, 2017
    FDA Examines Alternatives for Off-label Communications; Finds Them Wanting
  • Jan 29, 2017
    FDA Memo Examines First Amendment Implications
  • Jan 28, 2017
    FDA Lists Investigational Product Information Manufacturers Can Provide to Payors
  • Jan 28, 2017
    FDA Details How It Evaluates Product Communications Containing Data Not in FDA-required Labeling
  • Jan 27, 2017
    Kardashian Endorsements Raise Questions from NAD
  • Jan 25, 2017
    FDA Issues Two Draft Guidances on Medical Product Communications, Memo on First Amendment Issues
  • Jan 20, 2017
    Dietary Supplement Maker Cited for Website Claims
  • Jan 12, 2017
    Oregon Bill Requires Drug Cost Reporting
  • Jan 12, 2017
    Group Releases Recommendations To Aid Preapproval Information Exchange
  • Jan 12, 2017
    Court Denies Partial Judgment Motion That Raised First Amendment Issues
  • More

Good Clinical Practice

  • Aug 4, 2017
    Senate Approves Right-to-Try Bill
  • Aug 2, 2017
    AllTrials Survey Finds Company Trial Registration and Result Reporting Policies Vary Widely
  • Aug 2, 2017
    HHS Opens SACHRP Nomination Process
  • Aug 1, 2017
    EMA Issues Revised Guideline for FIH Trials
  • Aug 1, 2017
    Public Citizen Asks OHRP and ORO To Suspend and Review Red Blood Cell Transfusion Clinical Trial
  • Aug 1, 2017
    OHRP Plans To Provide More Data on Its Compliance Oversight Activities After HHS OIG Review
  • Jul 31, 2017
    SACHRP Makes Recommendations for Use of Broad Consent
  • Jul 31, 2017
    SACHRP Develops Proposed Template for Obtaining Broad Consent
  • Jul 31, 2017
    SACHRP To Examine Single IRB and HIPAA Exemption Issues in Revised Common Rule
  • Jul 31, 2017
    FDA’s First Patient Engagement Advisory Committee Meeting To Focus on Trials
  • More

U.S. Food Labeling

  • Mar 31,2011
    Product Recalls
  • Feb 28,2011
    U.S. District Court Dismisses 'All Natural' Labeling Case Against Snapple Containing HFCS
  • Feb 28,2011
    FTC Urged To Halt Vitaminwater's Immunity Claims
  • Feb 28,2011
    FDA Withdraws Guidance on Menu Labeling
  • Feb 28,2011
    Dietary Guidelines Document Offers New Narrative As Nutrient Targets Remain Mostly Unchanged
  • Feb 28,2011
    Beverages with Calorie Information on Front of Packaging Hit Store Shelves Nationwide
  • Feb 28,2011
    FDA Delays Enforcement on Phytosterols Claims
  • Feb 28,2011
    Suit Targets Nutella's 'Balanced Breakfast' Claim
  • Feb 28,2011
    Consumer Interest in Nutrition Facts Label Waning
  • Jan 31,2011
    USDA Issues Draft Guidance on Percentage Labeling of Organic Products
  • More

FDA Regulation & Enforcement

  • Dec 13, 2019
    House Drug Cost Bill Includes Mandate for Pricing in Television DTC Drug Ads
  • Dec 12, 2019
    Dr. Stephen Hahn Confirmed as New FDA Commissioner
  • Dec 12, 2019
    Investigator Vacancies, Other Factors Continue To Challenge FDA’s Foreign Drug Inspection Program
  • Dec 12, 2019
    Association Develops Labeling Standard for Plant-Based Meats
  • Dec 11, 2019
    OPDP Issues Third Warning Letter for 2019
  • Dec 10, 2019
    Senators Call for HHS OIG Investigation of Patient Assistance Programs
  • Dec 5, 2019
    CBD: To Be or Not To Be a Supplement Ingredient; Petition Seeks a Go-ahead From FDA
  • Dec 5, 2019
    GSK Sues BI Over Inhaler Marketing Claims
  • Dec 4, 2019
    Three CBD Product Manufacturers Face Class Action Suits in California Citing FDA Warning Letters
  • Nov 27, 2019
    Outcome Health Executives and Employees Charged in Connection with Advertising Scam
  • More

Medical Devices

  • Oct 18, 2013
    Guidant ICD False Claims Suit Settled for $30 Million
  • Oct 17, 2013
    Budget Deal Leaves Device Excise Tax Intact; AdvaMed Pledges To Continue Its Repeal Effort
  • Oct 10, 2013
    Summary of Compliance Dates Established by the Unique Device Identification System Final Rule
  • Oct 10, 2013
    Establishing a UDI System: The Basics
  • Oct 10, 2013
    Device Company Asks Court To Invalidate HHS OIG Declaration That PODs Are 'Inherently Suspect'
  • Oct 7, 2013
    Draft Guidance Describes Functionalities of GUDID
  • Oct 2, 2013
    With Government Shutdown, FDA Stops Accepting New Device Submissions Requiring User Fees
  • Oct 1, 2013
    Final Guidance on Mobile Medical Apps Provides Enforcement Discretion for Lower-risk Devices
  • Sep 20, 2013
    Final Rule on Unique Device Identification Released
  • Sep 19, 2013
    Study: Limiting Reimbursement for Medicaid DMEPOS Items to Medicare Levels Would Offer Savings
  • More

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