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EVENT DATE
Oct 2016
M T W T F S S
03040506070809
EXPO DATE
Oct 2016
M T W T F S S
03040506070809

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Type: Online Event
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What Effect Does ICH E6 R2 Have On Risk-Based Monitoring And Overall Quality Risk Management?

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EVENT DESCRIPTION

With the aim of improving efficiencies in trial conduct while ensuring participant safety, regulatory guidelines have recently undergone revision. The revision to the ICH Guideline for Good Clinical Practice (E6 R2) primarily addresses quality management with a focus on risk identification, evaluation, control, review and reporting. With the pending adoption of these revised guidelines, it’s time to evaluate how your organizational structure and processes will be affected.

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EVENT DETAILS

Primary Industry:
Clinical Pharmacology
Other Industries:
Clinical Pharmacology, Professional Healthcare
Audience:
Senior professionals from phama and biotech companies interested in learning more about the ICH e6 R2 revisions and the impact it will have on their organizations -
Directors of Data Management
Directors of Clinical Operations
Study Managers
Project Managers
Central Monitors
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