Phase 2 Studies
This module is part of the DIA Drug Development and Life Cycle Management eLearning Program. In the Phase 2 Studies module, learners will gain understanding of 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
Who should attend?
This module is designed for individuals who are new to, or changing roles, in the pharmaceutical and biotech industries. This module will also benefit professionals who work in the area of:
- Clinical Research
- Project Management
- Administrative Support
- Quality Assurance
- Regulatory Affairs
- Medical Writing
- Business Support
Upon completion of this module, learners should be able to:
- Outline the key objectives and activities of Phase 2 studies
- Describe the regulatory activities and decisions that occur during Phase 2 studies
- Examine risk-return decisions involved in Phase 2 studies