Greater Cincinnati: Webinar Replay: What You Need To Know from the 2018 FDA Imaging Guidance

Webinar Replay: What You Need To Know from the 2018 FDA Imaging Guidance

Please click here to purchase your contact hour.

Speaker Name:

• Richard Patt, MD, Co-Founder and Principal, RadMD

Target Audience:

• CRCs
• CRAs
• Investigators
• Data Managers (Site, Sponsor, CRO)

Program Description:
This course will focus on the FDA Guidance released in April 2018. The course will review the sections of the guidance document and provide you with an overall take home awareness of the current FDA feeling on using imaging in clinical trials. With the increase of utilization and complexity of imaging in clinicial trials, an understanding of FDA’s most current thoughts on the subject is critical.

Program Agenda:
6:00 – 6:30 pm – Registration & Networking
6:30 – 7:30 pm – Educational Presentation
7:30 – 8:00 pm – Q&A/Discussion

Learning Objectives:

1. Better understanding of the FDA guidance that relates to Clinical Trial Imaging Endpoint Processes
2. Highlight relevant issues specific to CRAs, site coordinators and nurses, and other trial personnel
3. Identify changes in FDA’s approach to utilizing imaging in clinical trials with this new guidance

Contact hours: 1.0 Contact hours have been applied for through ACRP.

Membership is not required for online registration of contact hours.

To receive contact hours: Purchase the contact hours, sign in at the event, and attend the program. Log on to the ACRP website then “My Courses” to complete the evaluation no later than 30 days following the event and obtain the online certificate.

Registration Cost:

• $0 Chapter Members 
• $0 ACRP Members
• $15 Non-Members

Contact Hour Cost:

• $0 Chapter Members
• $15 ACRP Members
• $30 Non-Members

Refund Policy: Not applicable