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MDCG 2020-7 Post-market clinical follow-up (PMCF) Plan Template. A guide for manufacturers and notified bodies
Current performance of COVID-19 test methods and devices and proposed performance criteria - Working document of Commission services
Joint Implementation/preparedness plan on the new Medical Devices Regulation 2017/745 (MDR)
Long term action plan for better implementation and enforcement of single market rules
Notice to stakeholders - Withdrawal of the United Kingdom and EU legislation in the field of supplementary protection certificates for medicinal products and plant protection products
GROW/F3 - Rolling plan 2018
GROW/F3 - Executive summary Rolling plan
European radio navigation plan (ERNP)
GROW/F3 - Rolling Plan ICT 2017 Executive summary
GROW/F3 - Rolling Plan for ICT Standardisation 2017
European Defence Action Plan
GROW/F3-Rolling plan 2016 ICT Standardisation - TFRP259r2 addendum RP2016 final
Communication on a European agenda for the collaborative economy
GROW/F3 - Rolling Plan 2016 ICT Standardisation brochure
GROW/F3-Rolling plan 2015 ICT Standardisation - TFRP213 addendum RP2015 final draft
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