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Examples of subject information letters available
To help investigators write a short and clear subject information letter, the CCMO published two examples of subject information ...
CCMO launches a new website
On 5 November 2018 the CCMO launched a new version of its corporate website ccmo.nl.
EU clinical trial portal expected to go live in 2020
The EU portal and database for clinical trials are expected to go live in 2020. This was announced by the European Medicines ...
Change in procedure competent authority
As competent authority, the CCMO has the task to check the European adverse reactions database, EudraVigilance, for suspected ...
Informed Consent Form template updated in line with GDPR
The template for the Informed Consent Form has been updated. The immediate cause for this is the amendment of the General Data ...
Answers to frequently asked questions about the European Clinical Trial Regulation
Set of European guidance documents for clinical trials
Guidance documents for clinical trials are available on the website of the European Commission.
Combining progress report with safety report in research with a medicinal product
In research with a medicinal product, the annual progress report may be combined with the annual safety report. The CCMO takes ...
New European ethical considerations for research with minors
New European documents with recommendations available for clinical trials
The European Commission has published three new documents with recommendations for clinical trials. The documents are the result ...