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Event Contacts

Andrew Juurinen
Xtalks Life Science Webinars
Toronto, ON m6g1x5
(416) 977-6555

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.

Not sure if you want to exhibit at or attend the What Effect Does ICH E6 R2 Have On Risk-Based Monitoring And Overall Quality Risk Management?? See the panels below to get the information you need to make an informed decision.

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Event Details

Conference/Event Dates: 10/05/2016 - 10/05/2016
Classification: B2B
Primary Industry: Clinical Pharmacology
Other Industries: Clinical Pharmacology, Professional Healthcare
Cost to Attend: Free
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

Booth Details

Booth Size Booth Cost   Available Amenities
No Exhibiting   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

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