News - Latest
89 news items
- Date
- Relevance
-
New Subject Information Sheet (SIS) template now available on the CCMO website
A new template (in Dutch) for the Subject Information Sheet (SIS) for subjects aged 16 and over (adults) is now available on ...
-
Dutch Trial Register (NTR) no longer available
The Dutch Trial Register (NTR) is no longer available. The National Trial Register, in which the CCMO Register and the former NTR ...
-
MREC NedMec ready for review of research files
As of 15 April 2022, MREC NedMec, the result of the merger of MREC AVL and MREC Utrecht on 1 January 2022, offers review of ...
-
Therapeutic vaccines now only reviewed by MRECs
Based on the Central Review of Medical Research Involving Human Subjects Decree ( Besluit Centrale Beoordeling), the assesment ...
-
New online tool makes CTR scope more transparent
The new Clinical Trial Decision Tool helps you to determine whether your study with a medicinal product falls within the scope of ...
-
CCMO kicks off programme on patient participation in clinical trials
To promote patient participation in clinical trials, CCMO is launching a programme to cooperate actively with other parties. ...
-
New EMA document for sponsors on CTIS
The European Medicines Agency (EMA) has published a new document on the Clinical Trials Information System (CTIS). The document ...
-
CCMO closed between Christmas and New Year’s Eve
Due to the holiday season, CCMO will be closed from Monday 27 December 2021 to Monday 3 January 2021.
-
Information EU Clinical Trial Regulation available on CCMO's website
On 31 January 2022, the EU Clinical Trial Regulation (CTR) 536/2014 will apply with new rules for research with medicinal ...
-
New directive makes use of Site Suitability Declaration (VGO) obligatory for research with a medicinal product as of 1 November 2021
CCMO’s directive on the assessment of the suitability of research centres (TGO) has been adopted and will apply to studies with ...