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Regulations for issuing extracts from the state register of medical devices
01.07.2026
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New testing procedures for medical devices
24.06.2026
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The Ministry of Industry and Trade proposes to transfer the confirmation of drug production stages to a registry format.
17.06.2026
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The Ministry of Health has updated its rules for monitoring the safety of medical devices: unification with the EAEU and the transition to digital standards.
10.06.2026
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The Ministry of Health has proposed postponing the deregistration of medical devices due to the lack of information about the authorized representative.
03.06.2026
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The Ministry of Industry and Trade will be granted the right to conduct unscheduled inspections of pharmaceutical manufacturers.
27.05.2026
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List of our company’s services in the field of pharmaceutical products registration.
20.05.2026
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Inspection of sterilization sites for medical devices in the EAEU: a one-time assessment instead of multiple inspections
15.05.2026
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The EAEU has approved unified approaches to inspecting medical device manufacturers.
06.05.2026
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Quality and effectiveness criteria for dietary supplements (DS)
29.04.2026
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Actions after a refusal to amend the registration dossier: what you need to know
22.04.2026
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New rules for dietary supplement distribution: The Ministry of Health has introduced medical supervision.
08.04.2026
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Paper certificate and Registry Records: Clarification from Roszdravnadzor
25.03.2026
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Post-Marketing Obligations of Medical Device Manufacturers: A Checklist of Key Actions
11.03.2026
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NEW RULES FOR MEDICAL DEVICES IN THE EAEU: WHAT HAS CHANGED?
04.03.2026
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The role and updating of information of the authorized representative in the medical device market: key steps in 2026.
25.02.2026
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Roszdravnadzor is expanding its program to monitor AI-enabled medical devices.
18.02.2026
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THE SIMPLIFIED REGISTRATION OF MEDICINES AND MEDICAL DEVICES HAS BEEN EXTENDED.
12.02.2026
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