GEOMETRIC DIMENSIONING AND TOLERANCING
Introduction Participants will be able to understand drawings with GD&T symbols. Case studies and hands-on exercises using specially selected drawings allow participants to use and apply the information learnt in the course. Participants may also bring company drawings for interpretation during live case studies. Duration 3 days | 9am – 5pm | 21 hours Who…
GR&R STUDIES (MEASUREMENT SYSTEM)
Introduction GR&R Studies is a method for evaluating and quantifying an existing gauge or inspection system. It determines if an inspection method or equipment produce acceptable, marginal or unacceptable results. It is often taken for granted that inspection results are true values with no errors. In reality, all inspection or gauge results are subject to…
IATF 16949:2016 Internal Auditor
Objectives: Acquiring the knowledge and skills for new internal auditors and experienced internal auditors who need to perform internal quality audits to IATF 16949:2016. • Identify linkages to quality management principles • Identify and apply the process approach • Demonstrate an understanding of ISO 9001:2015 and IATF 16949:2016 • Demonstrate an understanding of risk-based thinking…
IATF 16949:2016 Lead Auditor Training
Objectives: Acquiring the knowledge and skills gained to undertake and lead a successful IATF16949 Automotive Quality Management System audit. • Identify linkages to quality management principles in the context of ISO9001 and IATF16949 • Identify and apply the process approach • Demonstrate an understanding of ISO 9001:2015 and IATF 16949:2016 requirements • Demonstrate an understanding…
INTERPRETATION & APPLICATION OF 21 CFR 820
Introduction Title 21: Food and Drug Part 820: Quality System Regulation Current Good Manufacturing Practice (cGMP) requirements are set forth in this quality system regulation. The requirements in this part govern the methods used in, and the facilities and controls used for, the design, manufacture, packaging, labelling, storage, installation, and servicing of all finished devices…
INTERPRETATION & APPLICATION OF AIAG VDA INTEGRATED APPROACH TO FAILURE MODE AND EFFECT ANALYSIS (FMEA)
Objective This program is designed to equip the participants with the practical knowledge on the Interpretation and application of AIAG-VDA Integrated Approach To Failure Mode and Effects Analysis (FMEA) in order to enable them to develop Design FMEA, Process FMEA and Supplemental FMEA for Monitoring and System Response. Duration 2 days | 9am – 5pm…
Introduction to IATF 16949:2016
Objectives: Appreciation for ISO 9001:2015 and IATF 16949:2016, including the process approach, risk-based thinking, and an understanding of how it is necessary and valuable to your overall business management system. Identify linkages to quality management principles Demonstrate an understanding of the process approach Demonstrate an understanding of risk-based thinking Demonstrate an…
INTRODUCTION TO PROJECT MANAGEMENT
Introduction Projects and Project Management works involve a team of people contributing their diverse individual expertise toward achieving a common objective or goal. Successfully managing a project requires effective planning and adherence to the industry’s best practices in every step of the process. By understanding the fundamentals of project management, you will be better prepared…
ISO 13485:2016 MEDICAL DEVICES & IA TRAINING
Objectives ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. The functions & requirements of the ISO 13485:2016 Medical Devices standard. The understanding & implementing of the ISO 13485 Medical Devices standard…