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Holiday Inn London Kensington Forum

2017年10月17日 (火) 午後 12:30 - 2017年10月18日 (水) 午後 5:00

97 Cromwell Road, London, SW7 4DN, United Kingdom

A Comprehensive Review of Regulatory Procedures for New Drug Applications in the US

ONLY 5 SEATS LEFT! This course will enhance understanding and be beneficial to persons who work in clinical research, data management, biostatistics, basic research, project management and marketing.

SESSION 4: HOW TO SUBMIT A NDA AND ACTION ON APPLICATIONS

Session Chair(s)

Carol H. Danielson, DrPH, MS, RAC

Carol H. Danielson, DrPH, MS, RAC

President

Regulatory Advantage, LLC, United States

Michael  Hamrell, PHD, RAC

Michael Hamrell, PHD, RAC

President

MORIAH Consultants, United States

  • How to submit a new drug application
  • Electronic submissions
  • Processing an NDA
  • Amendments to an unapproved application
  • FDA actions on applications
  • Benchmarks: Prescription Drug User Fee Act (PDUFA) metrics

Speaker(s)

Carol H. Danielson, DrPH, MS, RAC

HOW TO SUBMIT A NDA AND ACTION ON APPLICATIONS

Carol H. Danielson, DrPH, MS, RAC

Regulatory Advantage, LLC, United States

President

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