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INNOVATION PARTNERSHIP: QUICK GUIDE FROM PRACTITIONERS
PUBLIC PROCUREMENT PROCEDURES AND INSTRUMENTS IN SUPPORT OF INNOVATION
Buying Social - a guide to taking account of social considerations in public procurement (2nd edition)
Guide on Articles 34-36 of the Treaty on the Functioning of the European Union (TFEU)
Guide on Articles 34-36 of the Treaty on the Functioning of the European Union (TFEU)
Guidance document for the application of Regulation (EU) 2019/515 of the European Parliament and of the Council of 19 March 2019 on the mutual recognition of goods lawfully marketed in another Member State and repealing Regulation (EC) No 764/2008
Guidelines for economic operators and market surveillance authorities on the practical implementation of Article 4 of Regulation (EU) 2019/1020 on market surveillance and compliance of products
Regulation (EU) 2016/426 on appliances burning gaseous fuels (GAR) - Guidance document in relation to point 3.7 of Annex I - Materials and parts of appliances/fittings in contact with food and water intended for human consumption
Conformity assessment procedures for protective equipment
MDCG 2020-12 Transitional provisions for consultations of authorities on devices incorporating a substance which may be considered a medicinal product [...] as well as on devices manufactured using TSE susceptible animal tissues
MDCG 2020-11 Guidance on the renewal of designation and monitoring of notified bodies under Directives 90/385/EEC and 93/42/EEC to be performed in accordance with Commission Implementing Regulation (EU) 2020/666 amending Commission Implementing Regulatio
ATEX 2014/34/EU Guidelines
MDCG 2020-5 Clinical Evaluation - Equivalence. A guide for manufacturers and notified bodies
MDCG 2020-6 Regulation (EU) 2017/745: Clinical evidence needed for medical devices previously CE marked under Directives 93/42/EEC or 90/385/EEC. A guide for manufacturers and notified bodies
MDCG 2020-7 Post-market clinical follow-up (PMCF) Plan Template. A guide for manufacturers and notified bodies
MDCG 2020-8 Post-market clinical follow-up (PMCF) Evaluation Report Template. A guide for manufacturers and notified bodies
Clarifications on the initiative of upload of software into radio equipment
Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context
Guidance on the applicable legislation for leave-on hand cleaners and hand disinfectants (gel, solution, etc.)
Smart Guide to cluster policy monitoring & evaluation
MDCG 2020-1 Guidance on Clinical Evaluation (MDR) / Performance Evaluation (IVDR) of Medical Device Software
MDCG 2020-2 Class I Transitional provisions under Article 120 (3 and 4) – (MDR)
MDCG 2019-8 v2 - Guidance document - Implant Card relating to the application of Article 18 Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices
MDCG 2018-1 v3 Guidance on BASIC UDI-DI and changes to UDI-DI
User guide for Directive 2005/36/EC on recognition of professional qualifications
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