Media Summary: Recorded by Colin Wilsher, this 72 minute Webcast takes a look at the For the first time in over 20 years, the International Council for Harmonization ( Patricia Leuchten, President and CEO at The Avoca Group, discusses how the clinical trials industry should interpret the

Taster Ich E6 R2 Step - Detailed Analysis & Overview

Recorded by Colin Wilsher, this 72 minute Webcast takes a look at the For the first time in over 20 years, the International Council for Harmonization ( Patricia Leuchten, President and CEO at The Avoca Group, discusses how the clinical trials industry should interpret the We will present different perspectives on

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TASTER:  ICH E6 (R2) Step 4 Webcast
Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance Trailer
ICH E6 (R2) Explained | GCP Guidelines for Clinical Research, Investigators & Medical Affairs
Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors/CROs/Clinical Investigator/Site
Webinar: ICH E6 (R2) Risk-Based Requirements 02132019
PCT TV: Implementing the ICH E6 R2 guidelines with Patricia Leuchten, CEO at The Avoca Group
Final ICH GCP E6 R2 Addendum Trailer
RBM Webinar 2 - What Could Go Wrong? ICH E6 R2, Investigative Sites and Risk Assessment
Final ICH GCP E6 R2 Addendum Overview of Changes Trailer
ICH E.6 (GCP) Addendum R2 Step 4 Overview
Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer
Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer
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TASTER:  ICH E6 (R2) Step 4 Webcast

TASTER: ICH E6 (R2) Step 4 Webcast

Recorded by Colin Wilsher, this 72 minute Webcast takes a look at the

Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance Trailer

Final ICH GCP E6 R2: Implementing Risk Management Approaches for Compliance Trailer

The most profound change in the updated

ICH E6 (R2) Explained | GCP Guidelines for Clinical Research, Investigators & Medical Affairs

ICH E6 (R2) Explained | GCP Guidelines for Clinical Research, Investigators & Medical Affairs

Discover the Essentials of

Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors/CROs/Clinical Investigator/Site

Final ICH GCP E6 R2 Addendum: Overview of Changes Impacting Sponsors/CROs/Clinical Investigator/Site

For the first time in over 20 years, the International Council for Harmonization (

Webinar: ICH E6 (R2) Risk-Based Requirements 02132019

Webinar: ICH E6 (R2) Risk-Based Requirements 02132019

February 13, 2019 ...

PCT TV: Implementing the ICH E6 R2 guidelines with Patricia Leuchten, CEO at The Avoca Group

PCT TV: Implementing the ICH E6 R2 guidelines with Patricia Leuchten, CEO at The Avoca Group

Patricia Leuchten, President and CEO at The Avoca Group, discusses how the clinical trials industry should interpret the

Final ICH GCP E6 R2 Addendum Trailer

Final ICH GCP E6 R2 Addendum Trailer

For the first time in over 20 years, the International Council for Harmonization (

RBM Webinar 2 - What Could Go Wrong? ICH E6 R2, Investigative Sites and Risk Assessment

RBM Webinar 2 - What Could Go Wrong? ICH E6 R2, Investigative Sites and Risk Assessment

We will present different perspectives on

Final ICH GCP E6 R2 Addendum Overview of Changes Trailer

Final ICH GCP E6 R2 Addendum Overview of Changes Trailer

For the first time in over 20 years, the International Council for Harmonization (

ICH E.6 (GCP) Addendum R2 Step 4 Overview

ICH E.6 (GCP) Addendum R2 Step 4 Overview

ICH

Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer

Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer

ICH GCP E6 R2

Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer

Final ICH GCP E6 R2: Impact on Clinical Data Management Trailer

ICH GCP E6 R2

Final ICH GCP E6 R2: Sponsor Quality Management - Risk-Based/Risk Management Requirements

Final ICH GCP E6 R2: Sponsor Quality Management - Risk-Based/Risk Management Requirements

ICH GCP E6 R2