Description
Research falling under the Medical Device Regulation (MDR) and/or ‘Medical Research Involving Human Subjects Act’ (WMO) must be reviewed beforehand by an independent committee of experts: the ‘Medical Research Ethics Committee’ (MREC or METc). Without an approval from this committee, the research may not start. The purpose of the review is to safeguard the rights, safety and welfare of the test subjects participating in this research. Therefore, the METc plays an essential role if you want to do a research study involving human subjects and test products for clinical applications.Periode | 19-jan.-2023 |
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Evenementstype | Conference |
Locatie | Groningen, NetherlandsToon op kaart |
Mate van erkenning | Regional |
Documenten & links
Gerelateerde inhoud
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Activiteiten
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Discover the World of Health Technology
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HTRIC Kick-off
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HTRIC Innovation Booster: Innovation in implant Workflow(s)
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HTRIC Innovation Booster: Boosting your drug delivery
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HTRIC Innovation Booster: Theranostics and imaging
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HTRIC Innovation Booster: Cancer treatment
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HTRIC Innovation Booster: Responsible development and implementation of AI
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HTRIC Innovation Booster: Rehabilitation
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HTRIC Innovation Booster: The path to success - Funding opportunities and start-up support
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HTRIC Innovation Booster: Challenges of new start-up companies within health technology
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HTRIC Innovation Booster: Mental disorders
Activiteit: Organising and contributing to an event › Professional