Quality Plan

A Quality Plan will be required for all construction products covered by the EU Construction Products Directive (89/106/EC) that are the subject of attestation of conformity (AoC) procedures relating to product certification or certification of factory production control, i.e. AoC levels 1+, 1, 2+ and 2.

The Quality Plan should specify the particular production operations necessary to ensure the continuing compliance of the certified product with the requirements of the harmonized European Product Standard. The document should be properly controlled and authorized for issue.

A copy of the Quality Plan and the factory production control documents should be submitted to the Notified (certification) Body for review. This may not necessarily be the same organization as currently provides quality management system certification to ISO 9000 to your company. In the case of the CPD, the Notified (certification) Body role within BSI is carried out by BSI Product Services, using BSI Global Quality Services to perform the inspections of factories and their FPC systems.

Once implementation of the FPC system has been assessed and accepted (and the relevant EC Certificate of Conformity issued), the quality plan should be retained on file and any proposed amendments should be submitted for clearance before being implemented.

General guidance for Quality Plan: The following provides general guidance on the contents of a quality plan that is likely to be acceptable in a majority of cases. The operations should be regarded as additional to those that would normally be carried out under a quality system to ISO 9000. It is emphasized that this envisages a standard situation that may not be applicable in all circumstances.

A Quality Plan must reflect the requirements of the relevant harmonized European product standard, particularly the Annex Z covering the provisions of CE marking and should include, but not be limited to, the following:

·         Specific raw materials and/or component specifications with the inspection and/or test criteria.

·         Details of the manufacturing process identifying critical stages, the in-process inspection procedures, limits of acceptance and rejection criteria. This should include, where appropriate, a process flow chart of the manufacturing and inspection stages.

·         Particular procedures for dealing with non-conforming product e.g. disposal, identification, segregation, corrective action.

·         Frequencies of tests on finished products and the test methods to be used.

·         Details of the further testing of samples in accordance with a prescribed test plan

·         Specific sampling requirements and related procedures.

·         Cross-references to the quality management system or FPC document.

·         Calibration of measuring equipment and special equipment used in the manufacturing process.

·         Where appropriate, the particular marking requirements of the product standard and the Directive.

·         Retention periods of records specific to the product concerned.