"Mēs izmantojam sīkdatnes, lai nodrošinātu jums labāku pārlūkošanas pieredzi. Nepieciešamās sīkdatnes ir vajadzīgas Padomes tīmekļa vietnes būtisko elementu atbalstam. Neobligātās sīkdatnes palīdz mums sagatavot anonīmus un apkopotus statistikas ziņojumus, lai labāk apmierinātu jūsu vajadzības.
Ar jūsu atļauju mēs izmantosim sīkdatnes, lai sagatavotu apkopotus, anonīmus datus par to, kā apmeklētāji pārlūko mūsu tīmekļa vietni un kādi ir viņu paradumi. Mēs izmantosim šos datus, lai jūs gūtu labāku pieredzi mūsu tīmekļa vietnes pārlūkošanā.
Nodarbinātības, sociālās politikas, veselības un patērētāju tiesību aizsardzības padome
Nodarbinātības, sociālās politikas, veselības un patērētāju tiesību aizsardzības padome, 2026. gada 16. jūnijs
Main results
European Biotech Act I: Directive
The Council agreed its negotiating position on the European Biotech Act I directive, which updates the rules on genetically modified micro-organisms (GMMs) and the processing of organs.
The proposed directive forms part of the European Biotech Act I, which seeks to strengthen the competitiveness of the EU’s biotechnology sector, particularly in the area of health.
Overall, today’s Council marks an important milestone for Europe’s health agenda. The progress we achieved will strengthen the EU’s competitiveness, resilience and capacity to act in the field of health. These achievements reflect the vision of the Cyprus presidency: ‘An Autonomous Europe, Open to the World’. A Europe that invests in innovation, strengthens its resilience, secures its strategic interests, and delivers for its citizens while remaining open to cooperation.
Neophytos Charalambides, Minister for Health, Republic of Cyprus
Ministers held a policy debate on the European Biotech Act I regulation, which seeks to establish a framework of measures to strengthen the EU’s biotechnology and biomanufacturing sectors, particularly in the area of health.
In particular, they shared their countries’ priorities for the Biotech Act I, and discussed ways that the act could be effective in helping to improve competitiveness in the EU and ensure greater access for patients and citizens to innovative products.
The Cyprus presidency presented a progress report on the proposed regulation simplifying the rules on medical and in vitro diagnostic devices.
The aim of the proposal is to address ongoing issues in the existing legislation, including excessive regulatory burden and uncertainty for companies, as well as unavailability of certain medical devices.
The presidency’s progress report takes stock of the discussions carried out at the technical level during the Cyprus presidency.
Under “other business”, EU health ministers received information on the recent Ebola Bundibugyo virus (BVD) outbreak in Central Africa; the critical medicines act; health conferences organised during the Cyprus presidency; the pandemic agreement; the urban waste water treatment directive; and the work programme of the incoming Irish presidency.
Šis materiāls šobrīd ir pieejams tikai šādā(s) valodā(s):
