Support mechanisms for non-commercial clinical trials | Level | |||||||
National | EU Level (Multinational) | Global | ||||||
Dedicated webpage |
| X | ||||||
Training courses | All investigators in the Netherlands from academic and hospital centers have to follow a mandatory course on regulatory requirements to conduct clinical trials:
| X | ||||||
Scientific advice | ||||||||
Helpdesk, regulatory, CTIS and ethics support | Regulatory, ethics requirements and CTIS support is available for non-commercial sponsors via the CTR mailbox (ctrccmo [dot] nl (ctr[at]ccmo[dot]nl)); phone +31703406700 and meetings (upon request); see also information in above section on scientific advice. In addition, there are regular meetings with ethics committees to discuss best practices and harmonise procedures. | X | ||||||
Other services by National Competent Authority | Scientific support is organised on a institutional level, with no insight on the specific details, same as the support for EU funding programs. On an institutional level some support is also given to register clinical trials in CTIS in case the sponsor is from an institute. | X | ||||||
Services by ethics committee | Sponsors need only pay one fee per clinical trial (redistribution done by the national competent authority). | X | ||||||
Public GCP support | ||||||||
Public research office | ||||||||
National funding and other financial support |
| X | X | |||||
Funding coordination and navigation of research infrastructure | ||||||||
Support identifying research networks | ||||||||
Other support mechanisms |
| X |