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The Westin Boston Waterfront

Aug 15, 2016 7:30 AM - Aug 18, 2016 5:00 PM

425 Summer Street, Boston, MA 02210

Regulatory Affairs: The IND, NDA, and Postmarketing

Session 4: Special Topics for Clinical Research

Session Chair(s)

Drusilla  Scott, PhD, RAC

Drusilla Scott, PhD, RAC

Vice President, Regulatory Affairs

Sobi, Inc., United States

Carol H. Danielson, DrPH, MS, RAC

Carol H. Danielson, DrPH, MS, RAC

President

Regulatory Advantage, LLC, United States

  • Adequate and Well-controlled Trials
  • Adaptive Study Designs
  • Comparative Effectiveness Research (CER)
  • Patient Reported Outcomes
  • Surrogate Endpoints
  • The Animal Efficacy Rule
  • Qualification of Drug Development Tools
  • Foreign Clinical Trials
  • Changes to the Investigational Drug
  • Financial Disclosure by Clinical Investigators

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