Clinical trials - legislation
Clinical trials - forms, instructions
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