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Advance GCP - Theory to Practice

 Date: 7th and 8th August 2009

 Venue: Mumbai

Course Description:

The two day workshop aims to provide practical application of GCP for important clinical trial processes. This program is designed for professionals with at least two years of experience in the clinical research industry.

Learner Objectives:

  • Review and update GCP knowledge
  • Recognize the challenges of site selection
  • Understand the issues involved in planning of clinical trial
  • Analyze ethics committee approval process
  • Assess acceptability of informed consent
  • Discuss monitoring aspects of protocol compliance
  • Comprehend identification and handling of safety issues

Faculty Objectives:

  • To arouse curiosity about the topic.
  • To explain concept of ‘Six Sigma’; its genesis and historical background.
  • To explain relevance of ‘Six Sigma’ & its applications in Clinical Research.
  • To sensitize the participants for a hands-on Workshop at a later date.

 Who Should Attend:

This course is recommended for experienced Clinical Quality Assurance Professionals, Clinical Research Associates, Project Managers, Investigators, and Study Coordinators.

Course Outline:

 Day 1:

 Time  Topic
 09.30 am - 10.30 am  GCP test and review
 10.30 am - 11.00 am  Tea Break
 11.00 am - 01.00 pm  Study Set up : Investigator selection
 01.00 pm - 02.00 pm  Lunch
 02.00 pm - 03.30 pm  Study Set up : Planning a trial
 03.30 pm - 04.00 pm  Tea Break
 04.00 pm - 05.30 pm  Monitoring 1 : Ethics committee approval

Day 2:

 Time  Topic
 09.30 am - 11.00 am  Monitoring 2: Informed consent process
 11.00 am - 11.30 am  Tea Break
 11.30 am - 01.00 pm  Monitoring 3 : Protocol Compliance
 01.00 pm - 02.00 pm  Lunch
 02.00 pm - 03.30 pm  Safety reporting
 03.30 pm - 04.00 pm  Tea Break
 04.00 pm - 04.30 pm  Open Session

 

Each topic had been handled as a case study / exercise / interactive discussion.


Conferences: