Jump to content

Investigators Guide to Investigator Site Audits Booklet

Price: USD ($) 13.00

Get the eBook now and gain instant access:

Buy this on Selz Selz powering ecommerce websites

The RQA is committed to the conduct of the highest quality clinical research. As part of that commitment, and for compliance with Good Clinical Practice (GCP) requirements, RQA has developed this guide to help investigators prepare and understand the activities and rationale for auditing investigator sites.


  1. Why are Audits Performed?
  2. How are Investigator Sites Selected for Audit?
  3. What is Good Clinical Practice?
  4. What will the Audit Involve?
  5. Investigator Site Audit Flowchart
  6. Regulatory Inspections
  7. Further Information


RQA GCP Committee 




February 2013

Discount Information

Discounts are available for bulk orders. Please enter one of the following discount codes:

  • BOOK10 for orders of 10 - 19 copies - 25% discount
  • BOOK20 for orders of 20 - 49 copies - 33% discount
  • BOOK50 for orders over 50 copies - 50% discount

This discount is available for both a block of one title or a combination of titles in hardback.

If ordering 50 or more books for delivery to outside the UK, please contact the RQA office as we will need to calculate the delivery cost for you.

Recommended Products


A Monitor’s Guide to Investigator Site Audits Booklet
Management of the Training and Competency of Personnel in GxP and Research Environments


C0021 GCP Auditing - Principles and Practice (24th Jun 2019 - 26th Jun 2019)
C9023 GCP Auditing - Principles and Practice (4th Mar 2019 - 6th Mar 2019)


Webcast - Where Does Audit End?

eLearning Products

Introduction to Good Clinical Practice (GCP) elearning