Quality Systems

Has your facility been producing a larger that usual amount of product that does not meet specification? Have you been having problems with determining where the problems with quality are coming from? Are you tired of customer complaints and costs of bad quality.

Implementation of an ISO 9001-2000 system will enable you to document your quality system and will also enable you to find the problem areas. This is done by systematically implementing a quality system that will evaluate all the areas of potential problems. This evaluation will also put in place procedures to prevent these problems if properly followed. There are also components of the system that will catch problems if they get past a breakdown in the other parts of the system.

A quality management system is of benefit no matter what product or service you provide. It can be detailed and certified by a registrar or parts of it can be put in place to obtain the improvements without going through the cost of registration.

CMA LLC can provide assistance in your quality system. We have experience in implementation of such systems as well as being trained and experienced in performing internal audits for quality systems.

Our services include:

	Evaluation of present system to determine the problem areas.
	Preparation of a documented quality system that will fit YOUR needs
	Auditing of your system to identify area of improvement and training your personnel to continue these audits and corrective actions.
	Consolidation of the quality system into environmental and health and safety management systems.
	Upgrade of your system to a TS-16949 system.

If you need an ISO 9001-2000 quality management system, or if you need the TS-16949 system since your parts are part of the final vehicle in automotive production, we can assist you in determining the most cost effective method of implementation. A quality management system not only improves your quality but can also identify process improvements that will improve your bottom line.

Certification to the ISO 9001-2000 or the TS-16949 standard can assist you in qualifying for additional opportunities due to the fact that an outside registrar has certified to your competence in these quality area. Even if you do not obtain certification, the analysis of your quality actions can greatly improve your quality and reduce your scrap rate and its costs.

Why not contact us to see how this type of system can be implemented in a cost effective manner and how it can improve your operations.

ISO 13485 – Medical Devices Quality Management System

Conformance Management Associates, LLC has assisted a number of clients in ISO 9001 and TS-16949 Quality Management Systems. In late July 2008, we became trained in internal auditing in ISO 13485. With a number of years experience in the medical and pharmaceutical fields, we can assist you in the implementation of your ISO 13485 system. We can also assist you in combining it with the ISO 9001 Quality Management System, ISO 14001 Environmental Management System and the OHSAS 18001 Health and Safety Management System.

The most cost effective way to implement these systems is to combine them into one system that covers all subject areas. It is less expensive and will be easier for your employees to implement and maintain. If you have any questions about this, please contact us.

Quality System Certifications

CMA is a certified ISO/TS 16949 Internal Auditor. View this certification
CMA is a certified ISO 13485 Combined Internal Auditor. View this certification