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Lock procedure for expensive medicinal products
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1
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34
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November 1, 2024
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Is the new EU pharma legislation a threat to academic drug development?
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0
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24
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September 20, 2024
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Looking for a detailed overview of the drug discovery, development and deployment journey of biologics?
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0
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25
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September 17, 2024
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Looking for a detailed overview of the drug discovery, development and deployment journey of small molecules?
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0
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37
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September 17, 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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21
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September 10, 2024
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Advice at HealthCare Institute (ZIN)
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1
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42
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September 9, 2024
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Data protection in personalized medicine
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0
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23
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July 31, 2024
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AI for drug combinations
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0
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20
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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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25
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August 21, 2024
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Market approval guidelines
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1
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23
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August 21, 2024
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Clinical trial application review
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1
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28
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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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20
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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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32
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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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24
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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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17
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May 30, 2024
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Language on the label
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0
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20
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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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13
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May 30, 2024
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SUSAR reporting
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0
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21
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May 13, 2024
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