Knowledge base
On reviewing applications of foreign manufacturers of medicines, medical devices and equipment and approving fees for issuing, amending, extending, re-issuing and duplicating the certificate
Sets how applications from foreign manufacturers or their agents are reviewed and the fees for issuing and changing their certificate.
- Act type
- Order of the Minister of Health
- No.
- 31
- Adopted
- 6 September 2024
- Ministry of Justice registration
- No. 3563, 24 October 2024
- Section
- Registration and dossier
Official text
On reviewing applications of foreign manufacturers of medicines, medical devices and equipment and approving fees for issuing, amending, extending, re-issuing and duplicating the certificate
Order of the Minister of Health · No. 31 · 6 September 2024
Related documents
- Presidential Resolution · No. PP-238 · 24 June 2026Checked against the official sourceImproving prevention, early detection and treatment of cancerMedical devices and equipmentMedicines
- Presidential Decree · No. UP-77 · 5 May 2026Checked against the official sourceImproving management efficiency in the healthcare systemMedical devices and equipmentMedicines
- Order of the Minister of Health · No. 2 · 14 April 2026Checked against the official sourceProcedure for inspecting the manufacturing conditions of medical devices during state registrationMedical devices and equipmentMedicines
- Cabinet of Ministers Resolution · No. 738 · 24 November 2025Checked against the official sourceState-registration procedures for medicines and medical devicesMedicinesMedical devices and equipment