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Template for annual safety report of investigator-initiated research with a medicinal product

In response to an initiative of UMC Utrecht, the CCMO has made a template available for the annual safety report for ...

News item | 31-01-2019 | 09:26

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 ...

News item | 14-01-2019 | 16:22

CCMO launches a new website

On 5 November 2018 the CCMO launched a new version of its corporate website ccmo.nl.

News item | 05-11-2018 | 00:00

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 ...

News item | 08-10-2018 | 13:03

Change in procedure competent authority

As competent authority, the CCMO has the task to check the European adverse reactions database, EudraVigilance, for suspected ...

News item | 28-09-2018 | 15:07

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 ...

News item | 09-05-2018 | 11:23

Answers to frequently asked questions about the European Clinical Trial Regulation

News item | 24-04-2018 | 10:11

Set of European guidance documents for clinical trials

Guidance documents for clinical trials are available on the website of the European Commission.

News item | 05-03-2018 | 15:37

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 ...

News item | 20-10-2017 | 13:45

New European ethical considerations for research with minors

News item | 20-10-2017 | 09:23