ISO/TS 14027:2017
Environmental labels and declarations — Development of product category rules
ISO/TS 14027:2017 provides principles, requirements and guidelines for developing, reviewing, registering and updating PCR within a Type III environmental declaration or footprint communication programme based on life cycle assessment (LCA) according to ISO 14040 and ISO 14044 as well as ISO 14025, ISO 14046 and ISO/TS 14067.
It also provides guidance on how to address and integrate additional environmental information, whether or not it is based on LCA in a coherent and scientifically sound manner according to ISO 14025.
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Symbols and abbreviated terms
5 Principles
5.1 LCA based environmental information
5.2 Involvement of interested parties
5.3 Comparability
6 PCR development
6.1 General
6.2 Consistent information
6.3 Comparability
6.4 PCR preparation
6.4.1 Formation of the PCR committee
6.4.2 Tasks of the PCR committee
6.4.3 Adaptation of existing PCR
6.4.4 Open consultation
6.5 Content of the PCR
6.5.1 Product category
6.5.2 Functional unit or declared unit
6.5.3 Requirements for conducting the underlying LCA or footprint studies
6.5.4 Predetermined parameters
6.5.5 Core rules and PCR
6.5.6 Conditions to support comparability
6.6 Additional environmental information
7 PCR review
7.1 General
7.2 The PCR review panel
7.3 Procedures
7.4 Tasks of the review panel
7.5 PCR review statement
8 PCR identification and registration
8.1 PCR identification
8.1.1 Identification of the PCR document
8.2 PCR registration
9 Updating, revision and expiration of PCR
Annex A (informative) Information modules
Annex B (informative) Tasks for the programme operator
Bibliography
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Symbols and abbreviated terms
5 Principles
5.1 LCA based environmental information
5.2 Involvement of interested parties
5.3 Comparability
6 PCR development
6.1 General
6.2 Consistent information
6.3 Comparability
6.4 PCR preparation
6.4.1 Formation of the PCR committee
6.4.2 Tasks of the PCR committee
6.4.3 Adaptation of existing PCR
6.4.4 Open consultation
6.5 Content of the PCR
6.5.1 Product category
6.5.2 Functional unit or declared unit
6.5.3 Requirements for conducting the underlying LCA or footprint studies
6.5.4 Predetermined parameters
6.5.5 Core rules and PCR
6.5.6 Conditions to support comparability
6.6 Additional environmental information
7 PCR review
7.1 General
7.2 The PCR review panel
7.3 Procedures
7.4 Tasks of the review panel
7.5 PCR review statement
8 PCR identification and registration
8.1 PCR identification
8.1.1 Identification of the PCR document
8.2 PCR registration
9 Updating, revision and expiration of PCR
Annex A (informative) Information modules
Annex B (informative) Tasks for the programme operator
Bibliography