ISO 9001: 2015 under revision: Standards for Organization

ISO 9001: 2015 under revision: Standards for Organization ISO 9001 very popular standard are used by billions of people  and millions of organization over the world, after success of the…

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5S Corrective Action Report

A 5S corrective action report is document use to proceeding actions to eliminate defects from the product or process. This report may includes a non-conformance details, root causes and solutions…

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Process change review checklist

Process change review checklist   What is Process change review checklist? Process change review checklist is document for verification of implemented changes in organization. A document covered new processes, machine,…

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Manufacturing Process Audit Checklist

Manufacturing Process Audit Checklist: Check sheet/ Template / Checklist Format What is manufacturing process audit? Manufacturing Process Audit Checklist is specifically defined checklist format for audit manufacturing processes and sequences,…

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Calibration Calendar for Instruments

Calibration Calendar for Instruments As basic requirements of QMS Systems (ISO 9001, TS 16949 etc..) having a clauses & needs of clauses in manual system that any organization which had…

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