BOX 3-3Disciplinary Components of Regulatory Sciencea

  • Basic investigation
  • Bioengineering
  • Bioethics
  • Bioinformatics
  • Biology
  • Bionutrition
  • Biostatistics
  • Chemistry
  • Clinical investigation and clinical trial design
  • Clinical pharmacology
  • Clinical research operations
  • Communication
  • Decision theory
  • Drug/device discovery and development
  • Drug disposition and metabolism
  • Economics
  • Epidemiology
  • Genetics
  • Government/policy
  • Information technology
  • IRB experience
  • Law
  • Medical informatics
  • Medicine
  • Metrics
  • Microbiology
  • Monitoring and quality assurance
  • Nutrition
  • Pharmacology (whole animal)
  • Pharmacy
  • Protection of human subjects
  • Public health
  • Regulatory knowledge
  • Research pharmacy
  • Risk assessment and communication
  • Surveying/methods
  • Systems analysis
  • Systems biology
  • Technology transfer
  • Toxicology
  • Veterinary
a

This box provides an integrated list of disciplinary components of regulatory science offered throughout the workshop by speakers and audience members.

From: 3, Defining a Discipline of Regulatory Science and Core Competencies for Its Workforce

Cover of Strengthening a Workforce for Innovative Regulatory Science in Therapeutics Development
Strengthening a Workforce for Innovative Regulatory Science in Therapeutics Development: Workshop Summary.
Institute of Medicine (US).
Washington (DC): National Academies Press (US); 2012.
Copyright © 2012, National Academy of Sciences.

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