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Drug precursors FAQ
List of National Competent Authorities for Cosmetics, Poison Centres and other relevant authorities
List of harmonisation legislation subject to Regulation (EU) 2019/1020
Is the European Union providing a regulatory model for other countries
National competent authorities responsible for the Fertilising Products Regulation
List of National Competent Authorities for Cosmetics, Poison Centres and other relevant authorities
Draft agenda - Detergents Revision Stakeholders workshop - 12 May 2022
Regulation (EU) 2016/424 application guide
Commission Regulation (EU) 2021/57 REACH Lead in gunshot in or around wetlands - National legislations - The Netherlands
Intention communicated by The Netherlands to prohibit placing on the market, discharging and carrying lead-containing gunshot throughout the territory
Inception Impact Assessment on the review of the Design Directive and Community Design Regulation
Unique Device Identification (UDI) System - FAQs
Declaration of interest (DOI) form - Call for expression of interest for expert panels on medical devices and in vitro diagnostic medical devices (2019/C 323/05)
Manufacturer incident report 2020
Manufacturer incident report for importing XML file with Adobe Professional 2020
MDR and IVDR implementing measures rolling plan
Changelog file 2020
Privacy statement - Call for expression of interest for expert panels on medical devices and in vitro diagnostic medical devices (2019/C 323/05)
State of play of joint assessments of Notified Bodies in the medical device sector
Study on workability issues concerning the implementation of Annex VIII of Regulation (EC) No 1272/2008 on harmonised information relating to emergency health response and preventative measures
MDCG 2019-15 GUIDANCE NOTES FOR MANUFACTURERS OF CLASS I MEDICAL DEVICES
MDCG 2019-13 Guidance on sampling of MDR Class IIa / Class IIb and IVDR Class B / Class C devices for the assessment of the technical documentation
MDCG 2019-14 Explanatory note on MDR codes
GS1 Basic UDI-DI
HIBCC Basic UDI-DI
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