Clinical trials

Name	Date of entry
Medicinal Products Act	24.11.2021	View
Conditions and Procedure for Conducting Clinical Trials of Medicinal Products	24.11.2021	View
Procedure for reporting serious adverse events occurring in clinical trials	24.11.2021	View
Rules of procedure of medical ethics committee for clinical trials	24.11.2021	View
Declaration of Helsinki	24.11.2021	View

Name	Date of entry
European Commission Guidelines	25.11.2021	View
Unique identifier using The Estonian Medicines Verification Organisation’s (REKS) web-based solution.	25.11.2021	View
Q&As	25.11.2021	View
The substantial amendments to the protocol and changes \| 37 KB \| doc	25.11.2021	Download
International standards of safety reporting apply	25.11.2021	View
The application is to be submitted in the EU format	25.11.2021	View
The signed declaration by the head of the health-care institution (study centre) \| 30.5 KB \| doc	25.11.2021	Download
Coordinated assessment of multinational CTAs through the Voluntary Harmonisation Procedure (VHP)	25.11.2021	View

Last updated: 25.11.2021