Course Description
The EU Clinical Trial Regulation (Regulation (EU) No. 536/2014) has ushered in a transformative era for clinical trials within the European Union and is built on three fundamental pillars: Enhancing the efficiency of clinical trials in Member States Concerned (MSCs) to foster innovation and reduce duplication, increasing the transparency of clinical trials across Europe, and prioritizing participant safety. At the core of this regulatory shift is the Clinical Trial Information System (CTIS), which serves as the central hub for all submissions to the EU. This comprehensive web seminar is designed to provide participants with a thorough understanding of the EU-CTR, its objectives, and its practical implications for clinical trial conduct in the EU.
Learning Objectives
Who Should Attend
Instructor
Andy Lawton
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Registration Fees
$735*
*Includes up to 20 participants per login at a single location. 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 logins for other locations, please call +1 781.972.5400 or toll-free in the U.S. 800.856.2556, or email customer.service@barnettinternational.com for pricing.
Accreditation Information
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 1 hours (0.1 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#: 0778-0000-24-034-L99-P. Released: 2/24.
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.