Knowledge base
MedicinesChecked against the official source
Additional measures to implement good practice (GxP) requirements in the pharmaceutical industry
Sets further measures to implement GxP requirements in the pharmaceutical industry.
- Act type
- Cabinet of Ministers Resolution
- No.
- 486
- Adopted
- 3 August 2021
- Section
- Quality, GxP and pharmacopoeia
Official text
Additional measures to implement good practice (GxP) requirements in the pharmaceutical industry
Cabinet of Ministers Resolution · No. 486 · 3 August 2021
Related documents
- Cabinet of Ministers Resolution · No. 472 · 7 September 2026Checked against the official sourceOn additional measures to improve legislation on technical regulationMedicines
- Order of the Minister of Health · No. 14 · 10 April 2026Checked against the official sourceProcedure for setting fees for GxP pharmaceutical inspection of pharmaceutical enterprises and preclinical and clinical research sitesMedicinesMedical devices and equipment
- Order of the Minister of Health · No. 13 · 16 December 2025Checked against the official sourceCertification-rule amendments covering GMP and ISO 13485 — No. 3386-2MedicinesMedical devices and equipment
- Order of the Minister of Health · No. 14 · 12 December 2025Checked against the official sourceDevelopment and inclusion of general and individual pharmacopoeial monographsMedicines