Overview

The Drug Development Phase 2 module is part of the DIA Drug Development and Lifecycle Management eLearning Program. In this module, learners will learn about the factors that drive the design and conduct of phase 2 clinical trials, as well as the activities and functional areas that contribute to a successful phase 2 program.

Estimated time to complete module: 1.25 hours

This eLearning module can be purchased individually or as part of the Drug Development and Lifecycle Management eLearning Program.

Featured topics

- Objectives and key players
- Regulatory activities
- Clinical R&D and biostatistics activities
- Case study part 1
- End of phase 2
- Case study part 2
- Review

Who should attend?

This module is designed for individuals who are new to, or changing roles in, the pharmaceutical and biotechnology industries. The module will also benefit professionals who work in the areas of:

Clinical Research
Project Management
Administrative Support
Quality Assurance
Regulatory Affairs
Manufacturing
Medical writing
Business Support

Learning objectives

Upon completion of this module, learners should be able to:
- List the key objectives and activities of phase 2
- Recognize the regulatory activities and decisions that occur during phase 2
- Identify risk-return decisions involved in phase 2

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Drug Development Phase 2

Overview

Featured topics

Who should attend?

Learning objectives

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