Knowledge base
Pharmacovigilance and medical-device safety monitoring
Procedure on medicinal-product pharmacovigilance and medical-device safety monitoring. This card points to the safety rules without restating reporting deadlines or assigning product-specific duties.
- Act type
- Order of the Minister of Health
- No.
- 18
- Adopted
- 30 December 2025
- Ministry of Justice registration
- No. 3752, 12 January 2026
- Section
- Safety and post-marketing control
Official text
Pharmacovigilance and medical-device safety monitoring
Order of the Minister of Health · No. 18 · 30 December 2025
Related documents
- Presidential Decree · No. UP-25 · 16 February 2026Checked against the official sourceAccelerating technical regulation reforms based on international practiceMedical devices and equipmentCosmetics
- Cabinet of Ministers Resolution · No. 628 · 4 October 2024Checked against the official sourcePost-marketing control of pharmaceutical productsMedicines
- Presidential Decree · No. UP-20 · 23 January 2024Checked against the official sourceAdditional measures regulating the pharmaceutical sector — UP-20Medicines