Risk Management & FMEAs
Many companies need to show that they have risk management documentation in place for products and for processes, in order to meet the requirements of the quality management system standards which apply to their industry.
However, when introduced at an early stage in the product development process a well designed risk management system can help to direct timely effort into product testing and design iteration. The net effect can be streamlined product introduction with a higher degree of product assurance at launch.
Similarly the use of Process FMEAs can identify the need for error proofing and quality checks at an early stage of process development. The use of data from related earlier products may enable the frequency of quality checking to be reduced on the new product. The net effect is an optimised process with lower rework and scrap levels resulting in a more cost effective and higher quality product.
DFM Projects has many years of experience in Risk Management with particular expertise in the Medical Devices and Automotive fields. We can help you to develop effective risk management processes whether for Risk Management Files, for Component and System FMEAs or for Manufacturing Process FMEAs.
We can organise and run the assessment meetings with your teams, and we can generate the Risk Management Files, Design FMEAs and Process FMEAs that you require.