Course Description
This web seminar provides a comprehensive overview of the FDA’s recently released draft guidance on Conducting Remote Regulatory Assessments (RRAs). Learners will gain a thorough understanding of RRAs, their implementation, and their impact on FDA-regulated industries. We will explore the key aspects of the guidance, including the types of RRAs, FDA’s expectations, and the potential consequences for regulated entities. By the end of the web seminar, attendees will be equipped with practical knowledge to navigate the evolving landscape of remote regulatory oversight.
Learning Objectives
Who Should Attend
Instructor
Elizabeth Ronk Nelson, M.P.H.
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Registration Fees
$835
Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: customer.service@barnettinternational.com
Accreditation Information
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1.5 hours (0.15 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will issue a receipt of completion for earned CEUs within three weeks of program completion. ACPE#: 0778-0000-25-021-L99-P. Released: 1/25.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.