ISO/TS TECHNICAL SPECIFICATION 14027 First edition 2017-04 Environmental labels and declarations Development of product category rules Marquages etdeclarationsenvironnementaux-Developpementdes regles de categoriedeproduit Referencenumber IS0/TS14027:2017(E) Intemational Organization for Standardization @IS02017 =ZHEJIANG INST OF STANDARDIZATION C1 5956617 Not for Resale, 2017/6/28 01:00:0 ted without license from IHS IS0/TS14027:2017(E) COPYRIGHTPROTECTEDDOCUMENT IS02017,Published inSwitzerland All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized otherwise in any form or by any means, electronic or mechanical, including photocopying, or posting on the internet or an intranet, without prior written permission. Permission can be requested from either ISO at the address below or ISO's member body in the country of the requester. ISo copyright office Ch. de Blandonnet 8. CP 401 CH-1214 Vernier, Geneva, Switzerland Tel. +41 22 749 01 11 Fax +4122 749 09 47 [email protected] www.iso.org Uicensee-ZHEJIANG INSTOF STANDARDIZRoISQl.7 -All rights reserved etworking permitted without license from IHS Not for Resale, 2017/6/28 01:00:0 Noreproduction IS0/TS14027:2017(E) Contents Page Foreword ..iv Introduction.. ... 1 Scope... 2 Normative references 3 Terms and definitions 4 Symbols and abbreviated terms ..4 5 Principles .4 5.1 LCAbasedenvironmentalinformation .4 5.2 Involvementofinterested parties 5.3 Comparability. .4 6 PCR development. .4 6.1 General .4 6.2 Consistent information .5 6.3 Comparability. .5 6.4 PCRpreparation. .5 6.4.1 Formation of the PCR committee .5 6.4.2 TasksofthePCRcommittee 6 6.4.3 Adaptation of existingPCR. .6 6.4.4 Open consultation. .8 6.5 ContentofthePCR .8 6.5.1 Product category. .8 6.5.2 Functional unit or declared unit. ..8 6.5.3 Requirements for conducting the underlying LCA orfootprint studies 6.5.4 Predetermined parameters .9 6.5.5 Core rules and PCR 6.5.6 Conditions to support comparability ..10 6.6 Additional environmental information. .10 7 PCRreview .11 7.1 General. .11 7.2 The PCR review panel .11 7.3 Procedures. ..12 7.4 Tasks of the review panel ..12 7.5 PCRreview statement .13 8 PCR identification and registration .13 8.1 PCRidentification. .13 8.1.1 IdentificationofthePCRdocument ..13 8.2 PCR registration. .15 9 Updating,revisionandexpirationofPCR ..15 AnnexA (informative) Informationmodules .16 AnnexB (informative) Tasksfor theprogrammeoperator ..18 Bibliography. .20 iii icensee=ZHEJIANG INSTOFSTANDARDIZATIONC15956617 d withoutlicense from IHS Not for Resale, 2017/6/28 01:00:07 No reproduction or networking perm