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Commission Implementing Decision (EU) 2020/1835Show full title

Commission Implementing Decision (EU) 2020/1835 of 3 December 2020 on the harmonised standards for accreditation and conformity assessment (Text with EEA relevance)

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Changes over time for: Commission Implementing Decision (EU) 2020/1835 (Annexes only)

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ANNEX IU.K.

1.Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices (OJ L 331, 7.12.1998, p. 1).U.K.

2.Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products and repealing Regulation (EEC) No 339/93 (OJ L 218, 13.8.2008, p. 30).U.K.

3.Regulation (EC) No 1221/2009 of the European Parliament and of the Council of 25 November 2009 on the voluntary participation by organisations in a Community eco-management and audit scheme (EMAS), repealing Regulation (EC) No 761/2001 and Commission Decisions 2001/681/EC and 2006/193/EC (OJ L 342, 22.12.2009, p. 1).U.K.

4.Commission Implementing Regulation (EU) 2018/2067 of 19 December 2018 on the verification of data and on the accreditation of verifiers pursuant to Directive 2003/87/EC of the European Parliament and of the Council (OJ L 334, 31.12.2018, p. 94).U.K.

ANNEX IIU.K.

NoReference of the standard
1.

EN ISO 14064-1:2019

Greenhouse gases - Part 1: Specification with guidance at the organization level for quantification and reporting of greenhouse gas emissions and removals (ISO 14064-1:2018)

2.

EN ISO 14064-2:2019

Greenhouse gases - Part 2: Specification with guidance at the project level for quantification, monitoring and reporting of greenhouse gas emission reductions or removal enhancements (ISO 14064-2:2019)

3.

EN ISO 14064-3:2019

Greenhouse gases - Part 3: Specification with guidance for the verification and validation of greenhouse gas statements (ISO 14064-3:2019)

4.

EN ISO 15195:2019

Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)

5.

EN ISO/IEC 17029:2019

Conformity Assessment - General principles and requirements for validation and verification bodies (ISO/IEC 17029:2019)

ANNEX IIIU.K.

NoReference of the standardDate of withdrawal
1.

EN ISO 14064-1:2012

Greenhouse gases - Part 1: Specification with guidance at the organization level for quantification and reporting of greenhouse gas emissions and removals (ISO 14064-1:2006)

1.7.2022
2.

EN ISO 14064-2:2012

Greenhouse gases - Part 2: Specification with guidance at the project level for quantification, monitoring and reporting of greenhouse gas emission reductions or removal enhancements (ISO 14064-2:2006)

1.7.2022
3.

EN ISO 14064-3:2012

Greenhouse gases - Part 3: Specification with guidance for the validation and verification of greenhouse gas assertions (ISO 14064-3:2006)

1.7.2022
4.

EN ISO 15195:2003

Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003)

1.7.2022
5.

EN ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories (ISO/IEC 17025:2005)

EN ISO/IEC 17025:2005/AC:2006

1.7.2021

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