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Section 6 :GCP Essential Documents of a Clinical Trial

Description: This section will reveiw the crucial GCP Essential Documents of a Clinical Trial.

You need to register for our course before you are given access to your course with a user name and password. Once you register this will be emailed to you at the email address that you provide to us.

Please click on the tabs to your right to go through the course in sequential order from the top to bottom tabs. Please begin your course by clicking the top tab to the right now! Good luck and enjoy this module! If you have any questions regarding the course please email us at info@clincoach.com or our lead trainer Paula Jones-Wright at pjwright@clincoach.com. You may also call us at any time at 902-463-9846.

Intellectual Property and Copyright Policy

Copyright©2007 by ClinCoach Inc. and Author Paula Jones-Wright. All rights reserved.

This statement reflects our ClinCoach Inc. Intellectual Property and Copyright Policy. No part of this course may be reproduced without prior written permission from Paula Jones-Wright.

No part of this course may be stored in a retrieval system or transmitted in any form or by any means electronic, mechanical, photocopying, recording or otherwise without prior written permission from Paula Jones-Wright.

Unauthorized use of our ClinCoach Inc. course content will violate applicable copyright and intellectual property laws. Breach of this ClinCoach Inc. policy will lead to legal action.

If you have any questions regarding the course please email us at info@clincoach.com or our lead trainer Paula Jones-Wright at pjwright@clincoach.com. You may also call us at any time at 902-463-9846.


   
  Clinical Research College Courses  
The courses are divided into sections. To complete an entire course you must finish all sections and pass the section quizzes. Once completed you will receive your Clinical Research College certificate.
  Good Clinical Practice in Clinical Research  
Section 1: An Introduction to Good Clinical Practice or GCP $99.99
Section 2: The Roles and Responsibilities of Ethics Committees $99.99
Section 3: The GCP Roles and Responsibilities of the Investigator $99.99
Section 4: The GCP Roles and Responsibilities of the Sponsor $99.99
Section 5 :GCP and the Clinical Trial Protocol and Protocol Amendments $99.99
Section 6 :GCP Essential Documents of a Clinical Trial $99.99
  Survivor Challenge for an FDA Audit and a GCP Inspection!  
Section 2: Preparation for a Good Clinical Practice Inspection and FDA Audit $99.99

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