Extension of the deadline for the ICF GCP R3 certification
The deadline for completing the ICF GCP R3 certification for [...]
Translation of certain documents used in the center into Serbian
In order to improve the work when conducting clinical trials [...]
Training of study teams on the new guideline – ICH GCP R3
Given that the new version of the GCP guideline (ICH [...]
Notice to sponsors and investigators affected by cyberattacks that may affect clinical trial data
In relation to possible cyberattacks, the Agency draws special attention [...]
Use of SMO type service provider services in RS
According to applicable local regulations as well as the Good [...]
Use of the FDA 1572 form for clinical trials in the RS – legal point
The instructions provided in the document with the title above [...]