•  The Office for Human Research Protections (OHRP) will be holding a special training session titled "Good Practices in the Conduct and Management of Human Research Studies" on June 4, 2008 from 9am - 12pm. The training be conducted by the law firm of Ropes and Gray. For more information, please contact the office of Human Research Protection at 504-988-2665 or via email at irbmain@tulane.edu

•  The FDA has published new guidance on Industry Computerized systems used in Clinical Investigations. Please refer to http://www.fda.gov/OHRMS/DOCKETS/98fr/04d-0440-gdl0002.pdf to view the document.