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Useful links about clinical development
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0
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29
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May 13, 2024
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CCMO symposium on academic drug development (NL)
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0
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50
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January 24, 2025
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Scientific advice for paediatric investigation plans (PIPs)
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2
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30
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March 24, 2025
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Platform Trials
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0
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12
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March 14, 2025
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Research Roadmap AmsterdamUMC useful for academic developers (not only in Amsterdam)
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0
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9
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March 13, 2025
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Overview of registries for rare diseases
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2
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12
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January 23, 2025
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How can I apply for a clinical study with product regulated under both CTR and IVDR (combined trial)?
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1
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9
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January 23, 2025
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How to include confidential information in CTIS?
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1
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9
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January 20, 2025
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CCMO webinar about the "Onderzoeksportaal" (NL)
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0
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10
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January 8, 2025
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How many participants are needed in my clinical First-In-Human (FIH) study to get a statistically sound answer?
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2
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27
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January 17, 2025
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Reimbursement of medication during clinical trial
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1
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16
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January 16, 2025
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JLABS - Road to first-in-human trials for small molecules (online and Leiden)
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0
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6
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January 9, 2025
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CCMO webinar about the new "onderzoeksportaal'
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0
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5
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January 8, 2025
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CCMO webinars over nieuw onderzoeksportaal
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0
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8
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January 8, 2025
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Guidance on Ethical, Legal, and Social Issues (ELSI)
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1
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16
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December 12, 2024
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Where can I ask for scientific advice for my clinical studies?
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1
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10
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September 10, 2024
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AI for drug combinations
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0
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8
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August 21, 2024
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Clinical trial for an extremely rare disease
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1
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11
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August 21, 2024
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Clinical trial application review
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1
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14
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August 21, 2024
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AI and prediction of side effects
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0
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3
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July 31, 2024
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Is it mandatory to include an IDMC/DSMB charter for the Dose Escalation Committee (DEC) for a phase I clinical study?
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0
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8
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July 2, 2024
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CTR - Is a legal representative required in the Netherlands
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0
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10
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May 30, 2024
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Retention period of data relating to traceability of ATMPs
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0
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4
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May 30, 2024
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Language on the label
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0
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11
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May 30, 2024
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Registration of unautorhised IMP in Extended EudraVigilance medicinal product dictionary (XEVMPD)
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0
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5
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May 30, 2024
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SUSAR reporting
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0
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9
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May 13, 2024
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