Ukrainian legislation on preclinical studies and clinical trials

29.10.2019 Updated 14.11.2025 37217 views

Guideline ‘Medicinal Products. Good Clinical Practice (GCP) ICH E6 (R3). ST-N MOZU 42–7.18:2025’, approved by Order of the Ministry of Health No. 1686 of 05.11.2025PDF · 1.4 MB · 22.10.2026

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MoH order No. 944 of 14 December 2009 ‘On Approval of the Procedure for Conducting Preclinical Study of Medicinal Products and Expert Evaluation of Preclinical Study Materials of Medicinal Products’DOC · 201 KB · 22.10.2026

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Guideline 'Medicinal Products. Good Laboratory Practice. ST-N MOZU :2008', approved by Order of the Ministry of Health No. 95 of 16.02.2009DOC · 254 KB · 22.10.2026

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Order of the Ministry of Health of Ukraine No. 690 of September 23, 2009 'On Approval of the Procedure for Conducting Clinical Trials of Medicinal Products and Expert Evaluation of Clinical Trial Materials and the Model Regulations on Ethics Committees'DOCX · 253 KB · 22.10.2026

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