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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
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