This workshop provides information across the full range of medical device clinical trial activities.

It is an ideal source of information for those new to clinical research and those requiring information specifically relating to regulatory and practical aspects of medical device clinical research.

Learning Objectives:

• Navigate the regulatory pathways for medical devices in the U.S
• Explore practical aspects of investigator and monitor selection
• Comply with the fundamentals of Good Clinical Practice (GCP)
• Explore practical aspects of conducting international clinical trials