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Advertising & Promotion

  • Apr 22, 2018
    District Court Dismisses Case Over Faxed Invitation To Free Dinner Discussion for Physicians
  • Apr 19, 2018
    Iowa AG Reaches Settlement with ‘Smart Pill’ Marketers
  • Apr 19, 2018
    Kentucky Sues J&J and Subsidiaries Over Opioid Marketing
  • Apr 19, 2018
    Allergan To Pay $3.5 Million To Settle Device Defect, Other Allegations Brought Under False Claims Act
  • Apr 18, 2018
    Sen. Sanders Introduces Opioid Marketing Bill
  • Apr 16, 2018
    N.J. Legislature Considers Bills Banning Drug Ads
  • Apr 16, 2018
    Small Study Finds Oncologists Receiving Payments More Likely To Prescribe Payors Drug
  • Apr 5, 2018
    Fast Talking, Complexity Cause Major Statement Concerns
  • Apr 3, 2018
    DOJ Moves To Participate in Opioid Lawsuit Settlement Discussions
  • Apr 3, 2018
    NAD Recommends ‘Cardio Miracle’ Supplement Discontinue Challenged Claims
  • More

Good Clinical Practice

  • Jul 28, 2018
    Protocol Complexity Hindering Trials
  • Jul 28, 2018
    FDA Finalizes Guidance Closing Orphan Loophole
  • Jul 27, 2018
    Survey Finds Few Clinical Sites Recruit at 100 Percent
  • Jul 27, 2018
    NIH Delays Registration and Reporting for Basic Science Studies Involving Human Subjects
  • Jul 27, 2018
    National Strategy Developed for Alzheimer’s Study Recruitment
  • Jul 26, 2018
    FDA Issues Draft Guidance on Diet in IEM Drug Trials
  • Jul 26, 2018
    ACRES Issues Trial Site Quality Standards
  • Jul 26, 2018
    FDA, OHRP Asked To Investigate Two Sedative Trials
  • Jul 25, 2018
    Vivli Trial Data-Sharing Platform Goes Live
  • Jul 23, 2018
    Patients Want to Know if Researchers Find Serious Concerns in Electronic Health Records
  • More

U.S. Food Labeling

  • Nov 7,2013
    Washington State Voting Results Indicate GMO Labeling Initiative Poised for Defeat
  • Oct 30,2013
    Meat Industry Appeals Ruling Over Agriculture Department’s Enforcement of COOL
  • Oct 23,2013
    AMI: Mechanically Tenderized Meat Proposal Should Be Cut
  • Oct 23,2013
    AMS Strikes Tartaric Acid from National Organics List
  • Oct 22,2013
    Beverage, Food Companies Spend Millions To Defeat Washington State GMO Labeling Efforts
  • Oct 17,2013
    ‘Most’ Furloughed FDA Workers Back at Job, Normal Operations To Resume Oct. 18
  • Oct 8,2013
    House Passes FDA-Specific Funding Bill, Measure Certain To Be Blocked in Senate
  • Oct 3,2013
    FDA Labeling Programs Stalled Over Budget Woes, USDA Programs Continue Operations, But Hobbled
  • Sep 26,2013
    Bill Pushes Front-of-Package Nutrition Summaries, Limits on Health and Nutrient Content Claim
  • Sep 19,2013
    CFSAN Priorities List Includes Changes To Nutrition Facts, Supplement Labeling Guidance
  • More

FDA Regulation & Enforcement

  • Jun 10, 2021
    Study Finds Even Meals May Influence Insulin Prescriptions
  • Jun 9, 2021
    11th Circuit: Florida Clinic’s Stem Cell Procedure Is Subject to FDA Regulation as an HCT/P
  • Jun 9, 2021
    Supplement Firm Asks Court To Dismiss Class Action
  • Jun 2, 2021
    Medicrea Settlement Continues Emerging DOJ Trend of Including Open Payments Violation Allegations in Settlements
  • May 28, 2021
    FDA, FTC Send Joint Warning Letters to Five Companies
  • May 27, 2021
    FDA’s Unapproved Drugs Initiative Is Reinstated; Updated Guidance on Enforcement Priorities Promised
  • May 26, 2021
    OPDP Encourages Grouped Electronic Submissions
  • May 26, 2021
    AMS Releases Results of 2020 NOP Enforcement Activity
  • May 20, 2021
    FTC Settles with CBD Marketer Over False Claims
  • May 20, 2021
    FDA Inspection Roadmap Reports COVID’s Impact, Outlines Factors That Will Set Future Priorities
  • More

Medical Devices

  • Jul 7, 2016
    FDA Offers Draft Guidance on Manufacturers' Release of Patient-Specific Device Information
  • Jun 29, 2016
    Device Manufacturer Penalized for ‘Apparent’ Violations of Restrictions on Exports to Iran
  • Jun 28, 2016
    FDA Final Biocompatibility Testing Guidance Stresses Risk Assessment, Use of Prior Data
  • Jun 21, 2016
    FDA Finalizes Guidance on Leveraging Adult Clinical Device Data for Pediatric Indications
  • Jun 18, 2016
    FDA Issues Draft Guidance on Evaluating and Reporting Age, Race, Ethnicity Data for Device Trials
  • Jun 16, 2016
    Draft Guidance Identifies Benefit, Risk Factors Considered by FDA When Dealing with Marketed Devices
  • Jun 15, 2016
    Final Rule Allows Stand-alone Symbols in Device Labeling; FDA Adds Options for Manufacturers
  • Jun 8, 2016
    National Academies Call on FDA To Explore Regulatory Pathways for OTC Hearing Devices
  • Jun 2, 2016
    Spinal Implant Device Maker Agrees To Settle Employee’s False Claims Act Allegations
  • May 31, 2016
    Draft Guidance Outlines FDA Categorization of IDE Devices for Medicare Coverage Decisions
  • More

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