DIA eLearning Programs:
NEW! Medical Affairs eLearning Program
Gain knowledge you need in elements of Medical Affairs including an overview of medical affairs, the role of the Medical Science Liaison, considerations for safety reporting, stakeholder engagement, development and planning of publications, compliance, and necessary actions for medical information professionals.
Medical Communications eLearning Program
This program contains relevant examples or scenarios designed to simulate medical information related tasks, so learners can apply the concepts to their day-to-day job responsibilities.
Drug Safety eLearning Program
This program includes six self-paced modules jam-packed with knowledge you need to know, from regulations and requirements through pre-market review and post-market monitoring.
Drug Development and Lifecycle Management eLearning Program
This six-module, self-paced program will help you understand the phases of drug development, major work streams, key players, and interrelationships necessary to develop new drugs in the US and Europe.
Clinical Trial Fundamentals eLearning Program
This three-module program is designed to provide a practical context to help clinical research professionals learn about conducting clinical trials.
Good Clinical Practice eLearning Module
This module provides the basic knowledge required to conduct clinical trials, including information about subject safety, regulations, and the practicalities of performing clinical research studies. It includes information about the recently adopted ICH GCP E6(R2) guideline.
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 ICH and the US FDA, as well as guidance for the creation and appropriate wording of these components.
