Table of Contents:
  • The path from bench to bedside
  • How did the FDA get to be in charge? The history of regulation of human drugs
  • The eureka moment: how new medicines are discovered
  • Test tube results are not enough: animal tests for a drug's utility
  • The business decisions: committing to development
  • Production of the new drug
  • Laboratory and animal safety testing
  • Getting set for clinical trials
  • Phase 1 clinical trials
  • Phase 2 clinical testing
  • Phase 3 testing
  • Putting together the application for approval: the new drug application (NDA)
  • Now everybody holds their breath (and some people may brush up on the rules for insider trading), will the FDA file the NDA?
  • The FDA review
  • What do outside experts think? The advisory committee meeting and FDA approval
  • The launch-marketing the drug
  • It's not over till it's over: post approval studies
  • Are we (well) served? Do we have the system of industry and regulations we need want and may deserve.