common specifications
as defined in Regulation (EC) No 106/2008 of the European Parliament and of the Council of 15…, Article 3, point (c) (Definitions)
(c)
‘Common Specifications’ shall mean the energy-efficiency and performance requirements, including testing methods, used to determine qualification of energy-efficient office equipment products for the Common Logo.
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Also defined in
- Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on harmonised rules on fair access to and use… 52022PC0068, Article 2, point (18)
a document, other than a standard, containing technical solutions providing a means to comply with certain requirements and obligations established under this Regulation - Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL LAYING DOWN HARMONISED RULES ON ARTIFICIAL… 52021PC0206, Article 3, point (28)
a document, other than a standard, containing technical solutions providing a means to, comply with certain requirements and obligations established under this Regulation - Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data… 32025R0327, Article 2(1), point (e)
laid down in Article 2, points (1), (12), (14), (22), (36) and (71), respectively, of Regulation (EU) 2017/745 - Regulation (EU) 2023/2854 of the European Parliament and of the Council of 13 December 2023 on harmonised rules on fair… 32023R2854, Article 2, point (42)
a document, other than a standard, containing technical solutions providing a means to comply with certain requirements and obligations established under this Regulation - Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical… 32017R0746, Article 2, point (74)
a set of technical and/or clinical requirements, other than a standard, that provides a means of complying with the legal obligations applicable to a device, process or system - Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending… 32017R0745, Article 2, point (71)
a set of technical and/or clinical requirements, other than a standard, that provides a means of complying with the legal obligations applicable to a device, process or system.