Διαχείριση της πολιτικής της ΕΕ για τη δημόσια υγεία

Improving health systems

Προαγωγή της καλής υγείας

Medical devices

Substances of human origin

Αίμα, ιστοί και όργανα

Φαρμακευτικά προϊόντα

Καταπολέμηση των ασθενειών

Εκτίμηση του κινδύνου

Επιστημονικές επιτροπές

Endocrine disruptors

Endocrine disruptors

Biocides

Biocides

Τελευταία ενημέρωση

26 Φεβρουάριος 2021

Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional
24 Φεβρουάριος 2021

COVID-19 tests: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19
18 Ιανουάριος 2021

Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
11 Ιανουάριος 2021

Covid-19: Commission Notice on audits to be performed by notified bodies
18 Δεκέμβριος 2020

Updated Implementation Rolling Plan - Regulation (EU) 2017/745 and Regulation (EU) 2017/746
18 Δεκέμβριος 2020

Updated - Ongoing guidance development within MDCG Subgroups
15 Δεκέμβριος 2020

MDCG 2020-18 - MDCG Position Paper on UDI assignment for Spectacle lenses & Ready readers
02 Δεκέμβριος 2020

MDCG 2020-17 - Questions and Answers related to MDCG 2020-4: “Guidance on temporary extraordinary measures related to medical device notified body audits during COVID-19 quarantine orders and travel restrictions”
01 Δεκέμβριος 2020

The EUDAMED Actor module is in production. On 1st December 2020 the European Commission has made available the Actor registration module to Member States and economic operators
13 Νοέμβριος 2020

Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746

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