The AMC1 21.A.139(d)(2) clarifies the control procedures covering the elements of Quality System should document the standards to which the production organisation intends to work.
An organisation having a quality system designed to meet a recognised Standard such as ISO 9001 (relevant to the scope of approval being requested) should expand it to include at least the following additional topics, as appropriate, in order to demonstrate compliance with the requirements of Part 21:
mandatory and voluntary occurrence reporting, as required by points 21.A.3A and 21.A.139(c) and continued airworthiness as required by point 21.A.165(e);
control of work occasionally performed (outside the POA facility by POA personnel);
coordination with the applicant for, or holder of, an approved design, as required by points 21.A.133(b) and (c) and 21.A.165(g);
issue of certifications within the scope of approval for the privileges of point 21.A.163;
incorporation of airworthiness data in production and inspection data, as required in points 21.A.133(b) and (c) and 21.A.145(b)
when applicable, ground test and/or production flight test of products in accordance with procedures defined by the applicant for, or holder of, the design approval;
procedures for traceability including a definition of clear criteria of which items need such traceability;
NOTE traceability is defined as : a means of establishing the origin of an article by reference to historical records for the purpose of providing evidence of conformity;
personnel training and qualification procedures especially for certifying staff as required in 21.A.145(d).
An Organisation having a quality system designed to meet a recognised aerospace quality standard will still need to ensure compliance with all the requirements of Part 21.
In all cases, the competent authority will still need to be satisfied that compliance with Part 21 is established.