Failure Mode and Effect Analysis

£100.00

Failure Mode & Effects Analysis (FMEA) has become a critical Six Sigma tool among businesses that are increasingly intent upon bringing more precision to solving their risk management challenges.

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Description

Failure Mode & Effects Analysis (FMEA) has become a critical Six Sigma tool among businesses that are increasingly intent upon bringing more precision to solving their risk management challenges. Design Failure Mode & Effects Analysis (DFMEA) is the procedure that determines where the design of the product, in particular, is most likely to fail and why, so actions can be taken to eliminate or reduce these risks. DFMEA is used before and during designing to prevent failures. Once the DFMEA is successfully documented, Process Failure Mode & Effects Analysis (PFMEA) should take place and followed by User Failure Mode & Effects Analysis (UFMEA) to ensure you remain in compliance.

Our templates are developed with consultants who have over 20 years of experience in the Medical Device industry and documentation that has been through successful audits. Our consultants are available, should you need further assistance in completing the documentation.