Day One
June 2, 2003
The Nuts and Bolts of the NIH SBIR/STTR Program

• Overview of NIH SBIR/STTR Programs
  Ms. JoAnne Goodnight, NIH SBIR/STTR Program Coordinator, (PowerPoint - 10 MB)
  
  
• Peer Review
  Dr. Anthony Coelho, NIH Review Policy Officer, (PowerPoint - 1.7 MB)
  
  
• Grants Management Processes & Issues
  Ms. Lisa Moeller, National Institute of Biomedical Imaging and Bioengineering, (PowerPoint - 345 KB)
  
  
• Indirect Cost Rate Negotiations & Audit Requirements
  Ms. Ruth Bishop, NIH Division of Financial Advisory Services, (PowerPoint - 151 KB)
  Ms. Leanne Robey, NIH Division of Financial Advisory Services, (PowerPoint - 62 KB)
  
  
• Regulatory Issues and Requirements: FDA Approval Process, Human Subject Protections, Animal Welfare Issues, Invention Reporting
  Mr. Paul Williams, FDA, (PowerPoint - 77 KB)
  Ms. Yvonne Higgins, DHHS Office of Human Research Protections, (PowerPoint - 81 KB)
  Dr. Axel Wolff, NIH Office of Laboratory Animal Welfare, (PowerPoint - 8 MB)
  Dr. George Stone, NIH Office of Extramural Research, (PowerPoint - 94 KB)

Day Two
June 3, 2003
Getting Products to Market

• From Academic Bench to Business
  Dr. Mary Pat Moyer, INCELL Corporation, (PowerPoint - 4.8 MB)
  
  
• Intellectual Property
  Ronald Kasner and Michael Gollin, Venable, LLP, (PowerPoint - 192 KB)
  
  
• Commercialization Strategy and Business Planning
  Rick King, PreFlight Ventures, (PowerPoint - 2.7 MB)
  
  
• Preparing a Commercialization Plan
  Dr. Jenny Servo, Dawnbreaker, (PowerPoint - 185 KB)
  
  
• Professional Society Assistance
  Mrs. Roberta Nixon, Society of Research Administrators (University of Virginia), (PowerPoint - 1.3 MB)
  Ms. Sara Jane Demy, Biotechnology Industry Organization, (PowerPoint - 645 KB)
  Dr. Ann Hammersla, Association of University Technology Managers, (PowerPoint - 2.7 MB)

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