หลักสูตรทั้งหมด

Hygienic design criteria. Material for equipment construction.Corrosion and surface treatment of stainless steel.Welding.Tank, connection, pump and valve in food industry.Cleaning in place – CIP.

 *** SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables leaners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***Regarding the increased automation, automotive driving, the 3rd edition of the AIAG Advanced Product Quality Planning (APQP) manual provides steps and tools to avoid quality problems in supply chain, improve customer satisfaction and support a continual improvement environment. This is a new opportunity for the automotive supply chain to pursue its commitment to excellence. While the main objective is still need of product conformity for series launch, the advantage of this new version is to reinforce managerial aspects by integrating model into the product development process. In addition, risk reduction / mitigation is strengthened, more upstream procurement planning and other key changes ensure a more comprehensive approach. This training shall provide and focuses on the key changes that you can expect from these new manuals

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables learners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***

*** SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables leaners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***Today’s laboratories demand professional finest quality equipment and consumables to give them a competitive edge. It is necessary to ensure that the instrument measurement is most useful and any information report also to determine in an accuracy of the instrument readings by others. In applying correction to instrument reading is a majority action which expected in effectiveness.

***SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables leaners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***

*** SGS also provide e-certificate and e-document (e-document will be provided for In-house training only). This enables leaners to be free from certificate loss, to reduce storage space, and ultimately to be environmental-friendly to which SGS’s current policy is attached.***This training provides you with an overview of requirements and interpretation of ISO 13485:2016, for medical devices quality management systems.During this training, we will provide you to overview of the purpose and requirements & interpretation of ISO 13485:2016. Our trainers will help you to understand the intent medical devices management system standards and to learn how to successfully apply the principles of quality management to your organization.

-Overview and review requirement of FSSC 22000 version 7 Standard -Introduction and guideline to internal audit and hygiene inspection for comply with FSSC 22000 version 7 Standard -Internal audit and hygiene inspection processes (Planning, Preparation, conducting audit, Audit conclusion and finding, CAR Writing, Audit report, Follow-up and Closed Out) + Workshop and Paper Examination 

- ข้อกำหนดระบบคุณภาพ ISO 9001 (Context, Leadership, Risk-based thinking ฯลฯ)- บทบาทและความรับผิดชอบของตัวแทนฝ่ายบริหารระบบคุณภาพ- การบริหารความเสี่ยงและโอกาส - การตรวจติดตามระบบคุณภาพภายใน การปฎิบัติการแก้ไขข้อบกพร่อง และการรายงานผลการตรวจติดตามระบบคุณภาพภายใน- การทบทวนโดยฝ่ายบริหาร- การเตรียมรับการตรวจประเมินจาก Certification Body (CB)