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Webinar 5 FEB Demystifying EU Regulations: Regulatory support tools for innovative medicines and technologies developers
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0
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19
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February 4, 2026
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Regulatory sandboxes: A new frontier for rare disease therapies (IRDiRC Publication )
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0
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24
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October 23, 2025
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Publication: A Regulatory Roadmap for Repurposing
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0
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36
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September 22, 2025
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Expert Class: Understanding the process of drug development CMC (Utrecht)
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0
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26
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September 17, 2025
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EMA Academia website updated
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0
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28
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September 8, 2025
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European Study on the Hospital Exemption out
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0
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91
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August 15, 2025
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Freedom to operate check - looking for a sparring partner
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4
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122
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August 5, 2025
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Would like to receive scientific advice from more than one national competent authority (NCA)? Use SNSA
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0
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24
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July 15, 2025
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Developing a NAM and thinking about interacting with the EMA? Check out the possibilities on the new EMA webpage
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0
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35
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July 11, 2025
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Final phase in the revision process of the new EU pharma legislation - what are your thoughts?
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2
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74
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July 1, 2025
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Lunch & Learn: The role of CMC in pharma start ups (Leiden)
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0
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24
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May 7, 2025
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Public consultation on current regulatory testing requirements for medicines and opportunities for the implementation of NAMs
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1
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50
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April 14, 2025
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Recently published - EMAs Horizon scan - New Approach Methodologies (NAMs)
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0
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41
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March 26, 2025
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What are the differences in regulatory pathways for obtaining approval for repurposed drugs in the EU, UK and US?
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0
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32
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February 25, 2025
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CBG Science Day 2025 - Platform Technologies: opportunities and challenges
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1
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45
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February 24, 2025
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Looking for tips and tricks for Paediatric Investigation Plan
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0
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25
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January 24, 2025
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The Innovation Race vs. Regulatory Pace | J&J webinar
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0
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25
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January 9, 2025
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What are the expected changes in the revision of the EMA guideline on radiopharmaceuticals?
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0
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34
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August 28, 2024
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What regulations and legislation I need to take in to account when registering a radiopharmaceuticals in the EU?
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0
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33
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August 28, 2024
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