ISO 9001:2015 is the international standards developed for manufacturing industry. We can say it is a certain criteria that every […]
How to get ISO 9001:2015 Certification for Manufacturing Companies? Read More »
As per IATF and QMS standard, there are a requirement of document and record control in our organization. Therefore, master
Master list of Documents & Records | Excel template Read More »
Every organization must have a contingency plan as per IATF 16949:2016 standards. It is a mandatory requirement of IATF. What
How Contingency Plan as per IATF 16949:2016 | with Example Read More »
Continual improvement is a primary objective of any organization. Every employee should adapt an improvement approach to grow personal as
Continual Improvement, Problem Solving & Error Proofing Procedure Read More »
This article explains the complete procedure of nonconformity and corrective action. Many quality engineers are thinking that the nonconformity are
10.2 Nonconformity and Corrective Action Procedure Read More »
Procedure for inspection and testing is crucial for monitoring and tracking good quality products. Inspection and testing are the methods
Welcome to our easy to learn guide on record retention procedure. It is an essential practice that every organization should
What is Record Retention? | Guidelines, Policy & Procedure Read More »
Procedure for Managing Calibration/Verification records is among the mandatory procedure for every organization as per automotive QMS (Quality Management System)
Procedure for Managing Calibration/Verification records Read More »
Procedure of training needs, awareness and competency is crucial in every organization. According to IATF 16949:2016 clause 7.2.1 organization should
Procedure of Training Needs Awareness and Competency Template Read More »
