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FAQ about inducements (Medical Devices Act)
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Guidance on the Management of Clinical Trial during the COVID-19 (Coronavirus) pandemic
Due to the corona crisis the source data verification for the majority of the clinical trials conducted is severely hampered. ...
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A: Relevant legislation
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B: Clinical investigations involving the use of medical devices – regime
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Requirements (re)start clinical trials
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Coronavirus (COVID-19): impact on the conduct of clinical trials under the Medical Research Involving Human Subjects Act (WMO)
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Greater cohesion and continuity needed in the care sector for people with chronic mental health problems
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IGJ information about clinical trials in the Netherlands
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Coronavirus (COVID-19): impact on the conduct of clinical trials under the Medical Research Involving Human Subjects Act (WMO)
The information below is valid during the COVID-19 pandemic until the situation is normalised and this is stated on the website ...
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Instruction to register the supply of alternative medical devices
A manufacturer, authorised representative, distributor, or importer can register the supply of an alternative medical device with ...