The protocol described below is referencing ISO DTR 19303-1. On-site audit should follow a standardized sequence of events beginning with an in-briefing between the BrandQ Expert, supplier project team leader, and participants. The in-briefing establishes the scheduled activities and responsibilities for conducting each activity. For example, all participating personnel should agree and confirm the standard, scope, and test files for the participants to process. Following the in-briefing, each of the areas identified in the scope of the audit will be assessed using the protocols described. During this phase of the audit, the supplier is expected to independently demonstrate its ability to operate a workflow conforming to the standard(s) selected.  If the supplier employed a consultant to assist in the preparation of the audit, the consultant is allowed to attend the audit, but only as an observer. The auditor will collect a series of test forms (processed files and printed samples) for color validation. This set of sheet will be sent to the Idealliance identified third-party independent laboratory for measurement and analysis. The person responsible for sampling should be identified during the in-briefing. All print samples must be initialed and timed. Print samples must be dried prior to shipment or handling.  以下描述的現場審核方案引用自ISO DTR 19303-1。現場審核應遵循標準化的事件序列，從BrandQ專家、供應商項目團隊負責人和參與者之間的簡報會開始。 簡報會上會介紹預定的活動以及進行每項活動的責任。例如，所有參加人士都應同意並確認供參加人士處理的標準，範圍和測試文件。 簡報完結後，每個審核範圍內選定的範疇將會以所述協議進行評估。在此階段的審核，供應商應獨立地展示其符合標準的工作流程的操作能力。 如果供應商聘請了顧問來協助審核的準備工作，該顧問可以出席審核，但只限於觀察員身份參加。 審核員會準備一系列的測試的文件（已處理的文件和打印的樣本）以進行色彩驗證。文件會發送到Idealliance同意的第三方獨立實驗室進行測量和分析。在簡報過程中應確認負責取樣的人員。所有打印樣本都必須簽署和記錄時間。打印樣品在運輸或處理之前必須確保是乾的。The in-briefing establishes the scheduled activities and responsibilities for conducting each activity. For example, all participating personnel should agree and confirm the standard, scope, and test files for the participants to process. Following the in-briefing, each of the areas identified in the scope of the audit will be assessed using the protocols described. During this phase of the audit, the supplier is expected to independently demonstrate its ability to operate a workflow conforming to the standard(s) selected.  If the supplier employed a consultant to assist in the preparation of the audit, the consultant is allowed to attend the audit, but only as an observer. The auditor will collect a series of test forms (processed files and printed samples) for color validation. This set of sheet will be sent to the Idealliance identified third-party independent laboratory for measurement and analysis. The person responsible for sampling should be identified during the in-briefing. All print samples must be initialed and timed. Print samples must be dried prior to shipment or handling. 

The Figure below shows applicable standards in each of the three steps of a packaging color reproduction workflow. This information was published on 12/12/2017 in the ISO/DTR 19303-1 Graphic Technology – Guidelines for Schema Writers – Part 1: Packaging printing colour reproduction.  以下圖片顯示了包裝與印刷色彩複製工作流程的三個步驟中每個步驟的應用標準。此信息於2017年12月12日發佈在ISO / DTR 19303-1印刷技術–構架作者使用指南–第1部分: 包裝與印刷色彩複製。
*CoA: Certificate of Analysis 分析證書
*CoC: Certificate of Conformance 合格證書

These international and national standards were referenced in constructing the BrandQ on-site audit process to ensure the practices and results are conformed to the highest standard of the industry. The number and title of each standard are listed below for quick referencing.  在構建BrandQ的現場審核流程時參考了這些國際和國家標準，以確保實踐和結果符合行業最高標準。下列為每個標準的編號和標題，以便參考。