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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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Mandatory update of instructions for generics and biosimilars: consequences of failure to comply
04.02.2026
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Tightening control over the circulation of antiseptics and dietary supplements through a labeling system
28.01.2026
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Reform of pharmaceutical legislation in the EEC: key changes and their significance
21.01.2026
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Draft new regulations for state registration of medical devices
14.01.2026
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How to determine if a product is medical?
17.12.2025
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New labeling deadlines for dietary supplements – what’s changing?
10.12.2025
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The Russian Ministry of Health is extending the simplified procedure for registering medicines and medical devices.
03.12.2025
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Russia is introducing strict measures against the online sale of dangerous dietary supplements.
27.11.2025
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Russia is transitioning to unified GMP rules within the Eurasian Economic Union.
19.11.2025
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