概览

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.

精选主题

- 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

谁应该参加？

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

学习目标

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

注册

Drug Development Phase 2

概览

精选主题

谁应该参加？

学习目标

获得信息并保持参与