- Evaluation of clinical trial applications and related documentation submitted by foreign and local sponsors in European Medicines Agency Clinical Trials Information System, and authorisation of clinical trials in Latvia;
- Supervision and control of clinical trials conducted in Latvia and assessment of the compliance with the requirements of Good Clinical Practice;
- Investigational drug safety monitoring within the cooperation network of European regulatory authorities;
- Evaluation of the submitted applications of observational studies using medicinal products and authorisation of observational studies.
