The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs 2015

The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs 2015 is an event dedicated to an overview of the requirement to obtain FDA permission to market a Medical Device products.

The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs 2015 covers topics such as:

• Preparing contents of the 4 types of 510(k)s
• Navigate the FDA medical device approval system
• Preparing contents of a PMA
• Preparing contents of an IDE
• Significant risk devices
• Non-significant risk devices

The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs 2015 brings together senior attendees involved or interested in:

• Quality Personnel
• Regulatory Affairs Personnel
• Research Personnel
• Clinical Personnel
• Auditors
• Manufacturing Personnel
• Personnel who require an understanding of the FDA Medical Device Approval Process
• Legal Personnel