All Stories

  1. Do patients trust the FDA?: a survey assessing how patients view the generic drug approval process
  2. Mandatory Disclaimers On Dietary Supplements Do Not Reliably Communicate The Intended Issues
  3. The Roles Of Academia, Rare Diseases, And Repurposing In The Development Of The Most Transformative Drugs
  4. Existing FDA Pathways Have Potential To Ensure Early Access To, And Appropriate Use Of, Specialty Drugs
  5. Restrictions On Pharmaceutical Detailing Reduced Off-Label Prescribing Of Antidepressants And Antipsychotics In Children
  6. Quantifying The Food And Drug Administration's Rulemaking Delays Highlights The Need For Transparency
  7. Secondary Patenting Of Branded Pharmaceuticals: A Case Study Of How Patents On Two HIV Drugs Could Be Extended For Decades
  8. The Food And Drug Administration Has The Legal Basis To Restrict Promotion Of Flawed Comparative Effectiveness Research
  9. Clinical Decision Support Systems Could Be Modified To Reduce 'Alert Fatigue' While Still Minimizing The Risk Of Litigation
  10. False Claims Act Prosecution Did Not Deter Off-Label Drug Use In The Case Of Neurontin