The Drugs Council is the responsible body for matters pertaining to clinical trials on medicinal products for human use in accordance with the Medicines for Human Use (Quality Control, Supply and Pricing) Law of 2001 (70(I)/2001).
The Clinical Trials Sector undertakes the management of Clinical Trials through the evaluation of applications for the initiation of clinical trials in Cyprus and of applications for substantial amendments after the submission of all required documents
Clinical Trials Regulation & CTIS
The way clinical trials are conducted in the European Union (EU) will undergo a major change when the Clinical Trials Regulation (Regulation (EU) No 536/2014) comes into application on 31 January 2022. The Regulation harmonises the submission, assessment and supervision processes for clinical trials in the EU through the Clinical Trials Information System (CTIS).
CTIS will be the single entry point for submitting clinical trial information in the EU and the European Economic Area (EEA). CTIS will contain a Sponsor workspace for clinical trial sponsors and the organisations that work with them, an Authority workspace for EU Member States, EEA countries and the European Commission, and a public website.
· The Sponsor secure workspace will assist clinical trial sponsors in preparing and compiling the clinical trial application and related documents to submit for assessment.
EU Member States and EEA countries will assess and supervise clinical trials in CTIS, while EMA sets up and maintains CTIS. The European Commission ensures the correct interpretation and implementation of the Clinical Trials Regulation.
· The Authority secure workspace will support the activities of EU Member States, EEA countries and the European Commission in assessing and overseeing clinical trials.
· Through the public website, members of the public can access detailed information on all clinical trials conducted in the EU and the EEA once trials start to be submitted and approved in CTIS.
The Clinical Trials Regulation foresees a 3-year transition period to CTIS.
EU Member States and EEA countries will have to work in CTIS from go-live, once applications are submitted.
· From 31 January 2022 until 31 January 2023, clinical trial sponsors can choose to submit their clinical trial applications under the Clinical Trials Directive (EC) No. 2001/20/EC through national submission processes, or under the Clinical Trials Regulation through CTIS.
· From 31 January 2023 all new clinical trial applications in the EU and EEA must be submitted under the Clinical Trials Regulation through CTIS.
· From 31 January 2025 trials approved under the Clinical Trials Directive that are still ongoing will have to be transferred to the Clinical Trials Regulation and to CTIS.
How clinical trials will be processed in CTIS
Clinical trial sponsors who want to gain regulatory approval for a clinical trial in one or more EU Member States and EEA countries will submit a single clinical trial application form and supporting dossier through CTIS. The submission of the single clinical trials application form and supporting dossier will also include the public registration of the clinical trial.
CTIS will support the day-to-day business processes of EU Member States, EEA countries and sponsors throughout the lifecycle of a clinical trial. It will provide regulatory oversight of clinical trials and tools for supervision and monitoring.
How to register for CTIS
Clinical trial sponsors that want to use CTIS must ensure their users have an EMA account. Users that have already an EMA account, for example to use Eudravigilance or the substances, products, organisations and referentials database (SPOR) do not need to create a new account. Users that do not have an EMA account can register via EMA Account Management.
Clinical trial sponsors may need to complete additional registration steps based on the user management approach they choose for CTIS. The organisation-centric approach allows for the management of users by an administrator at the organisation level rather than at the level of an individual trial. It is intended for organisations that will run several trials in CTIS. To make use of the organisation-centric approach, organisations must ensure they are registered in EMA’s Organisation Management System (OMS), and they must register a CTIS High Level Administrator via EMA Account Management.
How to prepare for CTIS
Clinical trial sponsors can consult the CTIS Sponsor Handbook for guidance on how to prepare for CTIS.
In addition, clinical trial sponsors can use the CTIS online training programme. The guide to the CTIS training material catalogue, which can be found on the training programme page on the EMA website, provides an overview of the training programme.
For more information on CTIS, visit the following page on the EMA Website:
For more information on training and support for the use of CTIS, visit the CTIS training and support page on the EMA website:
For information and training on the functionalities of CTIS, visit the online modular training programme page on the EMA website:
CTIS Sponsor Handbook:
For information on the Clinical Trials Regulation, visit Eudralex – Volume 10 – clinical trials guidelines:
EudraLex - Volume 10 - Clinical trials guidelines | Public Health (europa.eu)
Questions on CTIS functionalities can be directed through the CTIS User Support Service:
(link not yet available)