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Safe and correct use of food in interventional human studies - Guideline from the Netherlands Central Committee on Research...

In the Netherlands, the Central Committee on Research Involving Human Subjects (CCMO) recently published a guideline to clarify the requirements applicable to interventional studies with humans in the context of food,...more

New transparency rules for EMA’s Clinical Trials Information System (CTIS) - Clinical trial data disclosure in the EU

As of 18 June 2024, the Revised CTIS Transparency Rules as adopted by the European Medicines Agency (EMA) apply, and will impact patients, health care professionals and sponsors. Also as of 18 June, a revised version of the...more

Financial relations in the Dutch medical devices sector: investigations at hospitals and suppliers

On 21 September 2023, the Dutch Health and Youth Care Inspectorate (in Dutch: “Inspectie Gezondheidszorg en Jeugd”, IGJ) published a news report on financial relationships between physicians and medical device suppliers in...more

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