• Recent FDA Warning Letters:  What We Can Learn From Others' Mishaps
  (July 20, 2006)
  
  
• Informed Consent:  Why Patients Sue - A Review of Recent Litigation
  (September 21, 2006)
  
  
• Billing for Clinical Trials:  It's All In the Details (January 7, 2007)
  
  
• BSOM/PCMH Institutional Approval for Research:  Process Discussion and Trouble Shooting
  (March 15, 2007)
  
  
• Humanitarian Use Devices (HUDs):  Review of FDA Guidance and UMCIRB Procedures to Ensure Proper Use and Billing of HUDs
  (May 17, 2007)
  
  
• Protecting EPHI and Other Sensitive Data
  (July 19, 2007)
  
  
• Regulatory Update and Other Newsworthy Items
  (September 20, 2007)
  
  
• CMS's Decision to Forego the New Clinical Research Policy:  Implications for BSOM Clinical Trial Billing
  (November 15, 2007)
  
  
• Importance of Regulatory Documents:  Requirements and Practical Tips
  Guest Presenter:  Malissa Harris, RN, BSN
  (January 17, 2008)
  
  
• HIPAA Privacy Rules and Research
  (March 20, 2008)
  
  

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