Course content

    1. Welcome to Good Clinical Practice for non drug Clinical Research

    1. Session 1

    2. Why we follow GCP - the Nazi experiments

    3. Session 1 quiz

    1. Session 2a

    2. When participant safety by the Investigator is not the priority

    3. Session 2b

    4. Session 2 quiz

    1. Session 3a

    2. Negative participant experience of consent

    3. Session 3b

    4. Positive participant experience of consent

    5. Session 3 quiz

    1. Session 4

    2. Session 4 quiz

    1. Introduction to GCP R3 for non-drug trials - handbook

    2. Introduction to GCP for non-drug trials - feedback survey

About this course

  • $49.00
  • 4h of Study
  • 4 Lessons

Who you will learn with

Sophie Mepham

My expertise in the clinical trials sector is Global. I have worked in multiple clinical trial roles and have a deep understanding of how complex clinical trials are managed at site level. My Good Clinical Practice facilitator training with the National Institute Health Research in the UK in 2010 has taken me into hospitals, universities and research institutes across the world. I am an accredited Q-IAOCR Clinical Research Trainer and I have a Cert IV in Training and Assessment.

Sophie Mepham

My expertise in the clinical trials sector is Global. I have worked in multiple clinical trial roles and have a deep understanding of how complex clinical trials are managed at site level. My Good Clinical Practice facilitator training with the National Institute Health Research in the UK in 2010 has taken me into hospitals, universities and research institutes across the world. I am an accredited Q-IAOCR Clinical Research Trainer and I have a Cert IV in Training and Assessment.