related to the Marketed Substance In-process Quality Control are appropriate as a basis for change for a Marketed Substance - Production Chain entity:

• Table of current and proposed in-process tests as per B.I.a.4#2 req.
  the automatically assigned file name "vbia4-2-table-current-proposed-in-process-tests-substprodchain.pdf"
• Non-pharmacopoeial analytical method details as per B.I.a.4#3 req.
  the automatically assigned file name "vbia4-3-non-pharmacopoeial-analytical-method-details-substprodchain.pdf"
• Batch analysis data as per B.I.a.4#4 req.
  the automatically assigned file name "vbia4-4-batch-analysis-data-substprodchain.pdf"
• Justification for deletion of in-process test parameter as per B.I.a.4#5  req.
  the automatically assigned file name "vbia4-5-justification-for-deletion-in-process-test-parameter-substprodchain.pdf"
• Justification for new in-process test parameter as per B.I.a.4#6  req.
  the automatically assigned file name "vbia4-6-justification-for-new-in-process-test-parameter-substprodchain.pdf"
• In-process Quality Control - change - as per B.I.a.4 type ll req.
  the automatically assigned file name "vbia4-change-in-process-quality-control-1-type-ll-var.pdf"