Gentlemen,
Office for Technical Standardization, Metrology and State Testing launches new portal Placing products on the market. This portal provides users with detailed information on testing, metrology and standardisation, thus covering the technical harmonisation agenda. The portal is not only intended for SMEs, but will provide comprehensive information for testing bodies, standardisation professionals, consumers and manufacturers and other interested parties.
Access to the portal is free for all users.
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- REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL (EU) 2017/745 of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
- REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL (EU) 2017/746 of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU
On 27 December 2019, it was published in the OJEU:
Correction of Regulation (EU) 2017/746 of the European Parliament and of the Council
Correction of Regulation (EU) 2017/745 of the European Parliament and of the Council
They were published in OJEU L 117 on 3 May 2019:
Correction of Regulation (EU) 2017/745 of the European Parliament and of the Council
Correction of Regulation (EU) 2017/746 of the European Parliament and of the Council