The system implementation is a 7 steps process.

1) Gap Analysis
2) Management Review
3) Implementation
4) Training
5) Internal Audit
6) Corrections
7) Certification

At the beginning of a partnership we will perform a complete internal audit of the  existing Quality Management System and contrast the current system capability against all requirements of the applicable quality standard.


WHERE TO START?

OTHER SERVICES


The time required for a complete system implemendation greatly depends on the status of the existing QMS, the available of resources, current skillset and culture and most importuned:

THE WILLINGNESS TO CHANGE!


If we are confronted with a serious gap in the capability or resource availability within your organisation than IQMS can temporary fill the gap with one of our trained Quality Process Administrators until YOU and your team is ready to take over.


How long will it take?

               INOVATIVE   

            SCLABILITY

         SYSTEM DRIVEN

      COMPLIANT

   EFFECTIVE

RELIABLE

ENGINEERING support

NEW

POWERFUL

QMS TOOLS

AS9103

VARIATION MANAGEMENT OF KEY CHARACTERISTICS:

IQMS AS9102 inspection report incudes a statistical control sheet designed to estimates the current process capability, considering that the process mean may not be centered between the specification limits. The result of the measured process is measured in cpk charted and contrasted over a 6Sigme table. This is a great tool for understanding current process capabilities and proactively adjusting the sample size and method as needed. 

what's next?

SERVICES LIST

At the beginning of a partnership we will perform a complete internal audit of the  existing Quality Management System and contrast the current system capability against all requirements of the applicable quality standard.


.....creating a new standard for effectiveness

AS9102

INSPECTION REPORT:

IQMS custom inspection report is compliant with AS9101 and AS9102 requirements.
It includes statistical data analysis function and is:  1 capable to track critical dimensions  2 calculate CPK values  3 establish a Six Sigma reading 4 chart tool wear  5 create control limits  6 reference calibration data and  7 establish measurement and monitoring methods

INTEGRITY

Quality/Business Management System

SERVICES LIST

IQMS services include much more than training and quality system capabilities.

IQMS offers a wide range of innovative and powerful tools designed to mitigate RISK and assure product performance compliance and repeatability.

If your current TEAM does not have the time or has not jet acquired the appropriate skill level to create quality system tools such as the AS9102 report or pFMEA/Control planes than our stuff will fill the gap. 

pFMEA

PROCESS FAILUREMODE EFFECTIVENESS ANALYSIS:

A pFMEA is a structured analytical tool used by an organization, business unit, or cross-functional team to identify and evaluate the potential failures of a process. pFMEA helps to establish the impact of the failure, and identify and prioritize the action items with the goal of alleviating risk. It is a living document that should be initiated prior to process of production and maintained through the life cycle of the product.

Why choose to partner with us?

 

INTEGRITY Quality/Business Management System (IQBMS) is an industry leading quality system solution provider that is focused on INTEGRITY and SUSTAINABILITY.

One of the biggest risks to a business is allocating all Quality System responsibilities to one person.  

What would happen if this individual pursued new opportunities elsewhere?

Our approach to a fully integrated Quality Management System is to take all applicable Quality Requirements, communicate them into the Quality Assurance Manual and break them down into 5 distinct and independent Quality Process.

Every Quality Process will have an assigned fully trained and certified Quality Process Administrator who is capable of working within the requirements of the Quality System independently and effectively.

The performance and compliance of the individual Quality Process Administrator (QPA) will be monitored by us on a weekly bases and the integrity of the provided data will be verified on a monthly bases through internal audits.

 

This approach will enable YOU to rely on a system rather than individuals.