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Announcement about approval of the requirements for the responsible person of wholesale distributor for good distribution practice
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Announcement about approval of the requirements of labeling and packaging for medicinal products, pharmaceutical substances, herbal raw materials, investigational medicinal products, as well as for the patient leaflet, summary of product characteristics and trade names of medicinal products, and on excipients that must be indicated on the secondary packaging (Updated 07.02.2020)
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Training on ICH Stability Guidelines
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About Pharmacovigilance training which took place on July 9, 2019
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Information about the availability the SmPC and Package Leaflet in Armenian language in case of re-registration of medicines
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Information about documents accompanied to the registration certificate of the medicine
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Analytical Laboratory SCDMTE took the first place for interlaboratory comparative tests (professional testing - Proficiency testing study - PTS), organized by the international organization LGC
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Order 1997-А/29.06.2016 on medicine withdrawal from circulation
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Orders 1547-А/23.05.2016 and 1856-А/17.06.2016 on medicines withdrawal from circulation
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ISO/IEC 17025:2017
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