SAQ Supplier Self-Assessment Volume: The providers of medium and high risk in the risk assessment process should require them to write GeSI Supplier Self-Assessment Volume(SAQ). Including 5 major components: labor, health and safety(Health & Safety; Safe), Environs, Etics, and Management System.

VAP Validity Audit Program: This is the process of external inspection. That is, in addition to the internal audit of the provider itself, a third-party research certificate structure, such as SGS/Intertek / BSI, has been arranged to go to the provider for implementation verification. For example, if the on-site inspection operator is sure to wear safety gear, or whether the machine is equipped with anti-static functions to prevent cutting ... etc..

SVAP Improved Validity Audit Program(SVAP Validity Validity Validity Program): Adapted to Labor Facilities(such as factories) or Labor Provider(such as manpower agency or recruitment agency), Identify whether there is a risk of forced labor(Force Labor).

VAR Effectiveness Audit(VAR): The report that was approved after the SGS/Intertek / BSI agency went to the supply provider for implementation of the field audit. It is called Validation Audit Report(VAR).

CAR was audited by the supplier and proposed to improve the Preventive Action Report(abbreviated as CAR). Within 30 days of receipt of VAR, the manufacturer must submit a report on the improvement of the book and prepare a defense report based on the audit. The auditor of the factory will conduct a written audit and confirm the audit in the following year.