Course Overview

These courses provide a review of the clinical trial process. This series is different from many other courses in that its perspective is from that of the site based investigator rather than the sponsor. This series provides an excellent tool for the training and education of all members of the sponsor and clinical research teams to insure their knowledge and understanding of the clinical research process and GCPs. Included with each course is a downloadable, Student Guide containing the course script and a glossary of terms.

The Regulatory Context for Conducting Clinical Trials
Implementing A Clinical Trial Program
Ensuring Subject Protection and Scientific Integrity

Who Should Attend

  • Study site investigators
  • Site monitors and auditors
  • Research nurses
  • Regulatory affairs associates
  • Pharmacists
  • Data management personnel

Minimum Hardware Requirements
Windows 98/2000/NT/XP
Mac computer with an Intel processor
Pentium III processor at 500 MHz
128 MB RAM

Minimum Software Requirements
Web browser such as Google Chrome, Internet Explorer 6+, Safari
Adobe Acrobat Reader and Flash plug-ins
Access to the Internet with any connection 56K or above

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Course Details

3 Online Courses
4 Month Access
$590.00 Registration Fee

Ask a Question

Contact one of our course instructors to ask a specific question about the program.
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Our Students

  • 1 “After taking this series, I have a better Understanding of the process and plan to be more effective as a result.”

  • 2 “I now have a more in-depth understanding of my daily work.”