REGULATION (EU) 2017/ 745 OF THE EUROPEAN PARLIAMENT
???/???/???? As regards Article 168(4)(c) TFEU this Regulation sets high standards of quality and safety for medical devices by.
The European regulatory system for medicines
Rules and requirements applicable to pharmaceuticals in the. EU are the same irrespective of the authorisation route for a medicine. Transparency about how the
ICH and EU regulatory framework and the role of the European
Alberto Ganan Jimenez PhD – Quality of Medicines
COMMISSION DELEGATED REGULATION (EU) 2018/ 389 - of 27
???/???/???? supplementing Directive (EU) 2015/2366 of the European Parliament and of the Council with regard to regulatory technical standards for ...
Regulation (EU) No 347/2013 of the European Parliament and of the
???/???/???? on guidelines for trans-European energy infrastructure and repealing Decision No 1364/2006/EC and amending Regulations (EC) No 713/2009 ...
Joint Guidelines under Article 25 of Regulation (EU) 2015/847 on
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Communication from the Commission — Guidelines on the
???/???/???? (1) Regulation (EU) No 1286/2014 of the European Parliament and of the Council of 26 November 2014 on key information documents for packaged ...
Guidelines accompanying Commission Delegated Regulation (EU
???/???/???? Guidelines accompanying Commission Delegated Regulation (EU) No 244/2012 of 16 January 2012 supplementing Directive 2010/31/EU of the ...
Guidelines 05/2020 on consent under Regulation 2016/679 Version
???/???/???? 01) which were endorsed by the European Data Protection Board (hereinafter. “EDPB”) at its first Plenary meeting. This document is a slightly ...
Guidelines
???/???/???? regulatory technical standards on settlement discipline ... These guidelines are based on Article 6(2) of Regulation (EU) No 909/2014.
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