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Flowchart Adverse events research with a medical device
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Decree 2014 containing rules for compulsory insurance in medical research involving human subjects and explanatory memorandum
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CCMO Memorandum Flowcharts deferred consent for medical research in emergency situations
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Overview of assessment criteria described in MDR
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K3. CTA template – non-WMO research
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E1. Manual templates subject information sheets for research subjects <16 years of age (Dutch)
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K3. Template Clinical Trial Agreement - investigator-initiated research
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Simplified template of Annual Safety Report
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E1. Sample Subject Information Sheet
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K3. Template Clinical Trial Agreement - industry-sponsored research