ICH On-Demand Subscription
Don’t miss out on the latest ICH sessions from DIA conferences around the world.
The International Council for Harmonisation (ICH) of Technical Requirements for Pharmaceuticals for Human Use is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of drug development, manufacturing, and registration.
Throughout the year, new recordings will be added as they become available. Purchase a one-year subscription to get access to this library of dynamic, on-demand content. Get the information you need anywhere, anytime, on any device.
Current Recordings Include
- E6 and E8 Renovation Plan of Action
- Understanding ICH E6(R2) and the Impact to Clinical Trial Documentation and the Trial Master File
- E9(R1) Estimands
- E11 Pediatric Guideline Suite
- ICH Q12: Solutions to Facilitate Post-Approval Change Management Throughout a Product’s Lifecycle
- E17 Multi-Regional Clinical Trials
- E19 Optimizing Safety Data Collection
- Has the ICH Reform Been a Success?
- Overview of the Current ICH
- And More!
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Related eLearning Products
Clinical Trial Management Comprehensive eLearning Bundle
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Informed Consent: Comprehensive Concepts and Components eLearning Module
This comprehensive module provides the key concepts of informed consent. It explains the components of a complete and appropriate consent form as specified by the International Council on Harmonisation (ICH) and the US FDA, as well as guidance for the creation and appropriate wording of these components. It also includes a discussion on the benefits and concerns with electronic informed consent, and presents publications and projects that explore the use of eConsent.