ACT EU has launched a helpdesk to assist non-commercial sponsors in managing the EU clinical trial process. This helpdesk provides customized technical guidance on the Clinical Trials Information System (CTIS) and clarifies regulatory requirements throughout the clinical trial lifecycle. It can also consult with National Competent Authorities for case-specific support. Non-commercial sponsors can access this service by submitting a ticket through the CTIS Service Desk, identifying their “User affiliation” as non-commercial.1
You can register at the CTIS desk here.
References
- Home · EMA Account Management. (n.d.). https://register.ema.europa.eu/identityiq/home.html
Disclaimers
- The material in these reviews is from various public open-access sources, meant for educational and informational purposes only
- Any personal opinions expressed are those of only the author(s) and are not intended to represent the position of any organization(s)
- No official support by any organization(s) has been provided or should be inferred