Episode description
*This video is part of our educational video series on clinical trials. Clips will cover three key areas: clinical trial strategy, clinical trial execution, and regulatory expertise in clinical trials. Please reach out to RQM+ if you need support with clinical trials.*
🚨 Watch our newest video to learn best practices for 𝗮𝗱𝘃𝗲𝗿𝘀𝗲 𝗲𝘃𝗲𝗻𝘁 𝗿𝗲𝗽𝗼𝗿𝘁𝗶𝗻𝗴 𝗶𝗻 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝘁𝗿𝗶𝗮𝗹𝘀.
Manager of Safety Management Melanie Miller reveals:
📊 AE definitions for medical devices vs. drugs
🌍 Global reporting requirements and timelines
📋 Minimum data set for reportable AEs
🔬 Reporting differences across study types
Elevate your clinical trial expertise with RQM+ (this is the 21st video in our clinical trials-specific video series this year) and ensure regulatory compliance.
Reminder that you can find all of our clinical trial videos in other places, too. 👇
💼 LinkedIn
📺 The RQM+ YouTube channel
📧 For support with clinical trials, please contact us directly.
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📝 If you'd like to speak with us directly about how we might be able to support you and your organization, you're welcome to use our contact form.