Good Clinical Practice R2 addendum only


Instructor: Linda Hopkinson
Product ID: 706088

  • Duration: 90 Min
This webinar will provide you with a recap into what is Good Clinical Practice (GCP) and help you understand why the Revision 2 addendum was required. It will allow you to understand the implications of this revision for clinical research trials and gain the knowledge to fully comply with ICH GCP. It will provide an overview of what additions were added in the R2 addendum.
Last Recorded Date: Oct-2019


1 Person Unlimited viewing for 6 month info Recorded Link and Ref. material will be available in My CO Section
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Downloadable file is for usage in one location only. info Downloadable link along with the materials will be emailed within 2 business days
(For multiple locations contact Customer Care)



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Fax: +1-650-362-2367

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Read Frequently Asked Questions

Why Should You Attend:

Do you work in the clinical research industry? Is your knowledge and training on the guidance up to date and complete? Since the release of the ICH GCP addendum referred to as R2 there have been many changes made to the way clinical trials can be conducted. If individuals are not up to date with these requirements it will leave trials open to serious audit findings.

All individuals must hold a current ICH GCP certificate to work within clinical trials and if this hasn’t been completed since the R2 addendum was released you are no longer current.

Areas Covered in the Webinar:

  • What is GCP?
  • Recap on GCP guidelines
  • Why R2 revision was needed
  • Implications of update on future conduct of clinical research
  • Additions added to GCP in this addendum
  • Exercise on audit findings related to GCP
  • Examine reasons why this addition was important
  • Summary and conclusion

Who Will Benefit:

Clinical Research Professionals such as:

  • Clinical Research Associates
  • Clinical Project Managers
  • Clinical Trial Assistants
  • Clinical Research Organisation
  • Sponsors
  • Investigators
  • Research staff
  • Research nurses
  • Doctors
  • Dentists
  • Opticians
  • Pharmacists
  • Clinical research trainers
  • Site staff
Instructor Profile:
Linda Hopkinson

Linda Hopkinson
Clinical Research and Consultant, Bayer

Linda Hopkinson is a highly trained Clinical Research Professional with over 27 years of Research experience. Her experience encompasses Research nurse, Clinical Research Associate up to Project Management level before becoming a successful freelance worker and trainer. She has provided training for some of the top Sponsor companies as well as major CROs.

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Refund Policy

Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).




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