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Veronika Moravová
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Join date: Dec 4, 2023
Posts (5)
Apr 6, 2025 ∙ 2 min
ISZP - The Day After
Act No. 375/2022 Coll., on MDs and IVDs, stipulates that distributors and service providers listed in the Information System of Medical Devices (ISZP) must submit a change notification or confirm the accuracy of their data at least once a year—provided no changes occurred during the year. Otherwise, their activity in IZSP will be invalidated. Since ISZP has been launched in early March 2024, the first deadline to confirm data accuracy came at the beginning of last month.
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Mar 5, 2025 ∙ 2 min
Inconsistent VAT Rates for IVD Discussed at Roundtable
Subcommittee on Drug Policy, Medical Equipment, and Medical Devices hosted a roundtable discussion on VAT rates for IVD.
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Mar 30, 2023 ∙ 5 min
The European Commission's document on the new MDR transition periods addresses some contentious issues
On 20 March 2023, Regulation (EU) 2023/607 of the European Parliament and of the Council came into force, amending the MDR and IVDR. The...
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