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Drug Information Association
37th Annual Meeting 2001
Denver, Colorado


  1. The CDER 2001 Good Review Practices Initiative Clinical, Lisa Rarick

  2. The CDER 2001 Good Review Practices Initiative A General Overview, Michael Ortwerth

  3. e-CDER: A Look into the Future of Electronic Review, Melissa Chapman

  4. Electronic Common Technical Document in the FDA, Greg Brolund

  5. Electronic ICSRs-The US Pilot, Deborah Yaplee

  6. The Emergence of the Electronic FDA, Ralph Lillie, Director OIT

  7. FDA Information Technology: Accomplishments and Strategic Direction, Bill Bristow

  8. Giving your NDA Submission the Best Chance of Approval: The importance of Presentation, Lisa Rarick

  9. How to Build an Electronic Common Technical Document, Greg Brolund

  10. PhRMA IMPACC and the FDA: Update on PDUFA II Information Management Initiatives, Ron Conner

  11. Postmarketing Study Commitments, James Cobb

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