Protocol set up and management c-PCRs

For the set-up and management of a c-PCR to be declared applicable by Stichting NMD and to comply with the Assessment Method, a protocol has been developed by Stichting NMD. This protocol monitors the mutual consistency within and between the various material and product groups when c-PCRs are prepared. It is very important to emphasise that the c-PCR must be a detailed elaboration of the Assessment Method and standard EN15804, without deviating from it.

In those cases where a European (sub)process has already been established for the preparation and management of c-PCRs, it is important that this European (sub)process is followed.

The application form below should be completed by the initiator of the c-PCR.

Application form c-PCR

Type c-PCR: *

New PCR
• Update of PCR: give name and registration number below

Name and registration number update PCR:

Proposed scope: *

Have you checked that no validated c-PCR has been established for this product/material category?: *

If a c-PCR already exists, justify why this c-PCR is being initiated and should be drawn up:

Name of contact person initiator: *

Email: *

Organisation: *

Implementing organisation: *

Experience and references implementing organisation: *

Description of the participating organisations in the work group: *

What is the general plan regarding the drawing up of the c-PCR? At quarterly level, please give the planned start of the various phases:

Initiation phase: *

Collect data and establish calculation rules: *

Draw up c-PCR: *

c-PCR consultation round: *

Submit c-PCR: *

Do you agree with the privacy statement? *

Yes, I agree

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