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Clinical Trials for Pharmaceuticals: Design and Development November 2010

Nov 29, 2010
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Course Description

This course addresses the issues in the design of pharmaceutical clinical trials (including protocol development) and the interface of clinical trial design with the drug development process.

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Learning Objectives

  • Describe the clinical trial design process
  • Review key ethical considerations in clinical trials
  • Key components of protocol development
  • Requirements for the Investigational Plan
  • Describe the clinical trial phases

Who Should Attend

  • CRAs
  • Clinical Personnel
  • Regulatory Personnel
  • Quality Personnel
  • Manufacturing Personnel
  • Project managers
  • Those who require an understanding of clinical trial design

Instructor 

Albert A. Ghignone, M.S., R.A.C.

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Course Length Time

3 hours; 12:30 - 3:30 p.m. Eastern

Course Dates 

November 29, 2010                                 

Hold this course at your company!
For more information, contact Naila Ganatra at (215) 413-2471.

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PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)