On approval of the rules for the assessment of materials and compliance of preclinical (non-clinical) studies with Good Laboratory Practice (GLP) requirements of the Republic of Kazakhstan and/or the Eurasian Economic Union within the framework of pharmaceutical inspection
New Unofficial translationOrder of the Minister of Healthcare of the Republic of Kazakhstan No. KR DSM-181/2020 of November 4, 2020. Registered with the Ministry of Justice of the Republic of Kazakhstan on November 5, 2020 under No. 21596
Parameter |
Value |
|---|---|
| Act approved on | 11/04/2020 |
| Act change date | |
| Date of official publication in ILS "Adilet" | |
| Information on official publication of the act | 100000000031 |
| Act form | Rules, Order |
| Legal relations area | Providing population with medicines and medical products |
| Legal validity | Акт Министерства или ведомства |
| Agency of act regulation | The Ministry of Health of the Republic of Kazakhstan (previous name: the Committee of Health of the Ministry of Education, Culture and Health of the RoK; the Committee of Health of the Ministry of Health, Education and Sport of the RoK; the Agency of the RoK on Health Affairs) |
| Area of activity | Республика Казахстан |
| Act registration number in the State Register of Regulatory Legal Acts of the Republic of Kazakhstan | 148217 |
| RLA registration number assigned by rule-making body | ҚР ДСМ-181/2020 |
| Number of RLA state registration at justice agencies | 21596 |
| RLA developer | |
| Registered in the MoJ on | |
| Database section | Health care |
| Authority of departmental act registration | The Ministry of Justice of the Republic of Kazakhstan |
| Location of act approval | 100050000000 |
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