North Carolina Regulatory Affairs Forum

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Excited to see the NCRAF bringing together experts in regulatory affairs! This is such a great opportunity for anyone looking to deepen their understanding of the industry. 🌟
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Just registered for the 2024 RAC Workshops! Can't wait to learn more about the intersection of science and compliance. This is exactly the kind of professional development we need! 🙌
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Poslední diskuze

1. What are the key differences in regulatory requirements for lab-developed tests between the US and EU, and how do these differences impact innovation in the field?
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2. How can the collaboration between medical writing and regulatory affairs enhance compliance and streamline the approval process for new therapies?
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North Carolina Regulatory Affairs Forum
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NCRAF Upcoming Events Lab Developed Tests US and EU Perspectives Bridging Science and Compliance The Synergy between Medical Writing and Regulatory Affairs Become a membertoday to be notified as additional events are planned. Registration for the 2024 RAC Workshops are STILL OPEN. You must be a member to register standard membership is currently 50. Workshop registration is 75 This workshop series is a comprehensive overview of regulatory requirements for development manufacture marketing and compliance for drug and biological human medicines in the US EU and other countries.

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