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  6. Introduction to FMEA Using APIS IQ

Introduction to FMEA Using APIS IQ

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FMEA software "APIS IQ-FMEA/IQ-RM"

last updated:Jul 06, 2026

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FMEA - Introduction of Case Studies Using Automated Driving Monitoring Systems

[Steps in APIS IQ] FMEA consists of seven steps. Here, we will focus on the three most important and fundamental steps for conducting FMEA: structural analysis, functional analysis, and failure analysis. 1. Planning and Preparation: FMEA Scope Analysis 2. Structural Analysis: Create a structure tree from the selected system elements 3. Functional Analysis: Describe the "functions" of the system elements and create a function network 4. Failure Analysis: Describe the "failures" corresponding to the functions of the system elements and create a failure network 5. Risk Analysis: Management responsibilities, failure ranking: AIAG/VDA form / AP correspondence 6. Optimization: Measures to mitigate risks: AIAG/VDA form / AP correspondence 7. Documentation: Output and communication of results: AIAG/VDA form For more details, please check below. https://www.hulinks.co.jp/support/apis/gs/index.html

    Process Control SystemOther production management systems
APIS_intro.png

Introduction to FMEA Using APIS IQ

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APIS_intro.png APIS_0.png APIS_1.png APIS_2.png
  • Related Link - https://www.hulinks.co.jp/support/apis/gs/index.ht…
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[Basic Information] Other Features - Prevention of omissions through copy and paste of sheets - Tracking of items due to design derivations and design changes - Correspondence of different FMEA forms based on destination and client - Centralized management of mandatory items in accordance with various standards - Absorption of variations in wording by input personnel - Standardization of data across various quality management methods and tools other than FMEA - Support for communication with overseas clients (clarification of procedures) [APIS IQ 8.0 New Features] - Function enhancement: "Failure Naming Patterns" - More user-friendly AIAG/VDA form design - Improvement of management reports - Individually obtainable calculation strategies (FuSa) - New import and update options for FMEDA parameters within forms - Strengthening of variant permissions - Efficient and secure management via CDM Server, etc. https://www.hulinks.co.jp/software/quality/apis/section02/section01#s03 *For more details, please refer to the PDF document or feel free to contact us.

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It is software that is fully compliant with AIAG&VDA FMEA, with a wealth of sales and implementation experience at over 2,000 companies globally, including BMW, Continental, Daimler, DENSO, and Robert Bosch, across Europe, the United States, and Japan.

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Package Function Comparison Table https://www.hulinks.co.jp/software/quality/apis/section02

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Quality management tool 'APIS IQ' that enables failure analysis.

Quality management tool 'APIS IQ' that enables failure analysis.

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[Hulinks Blog] Risk Management for Medical Devices Using APIS IQ (FMEA): A Case Study of Cardiovascular Catheters

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ISO 14971 is an international standard for the systematic management of risks related to medical devices. APIS IQ-Software is one of the representative tools that supports risk analysis in FMEA and ISO 14971. Originally developed as a tool for the automotive industry, it can also be utilized for risk management in medical devices. In this article, we will specifically explain a series of processes for efficient implementation. □Risk Management for Medical Devices (FMEA) Using APIS IQ□ (Visit the HuLinks blog page) https://www.hulinks.co.jp/2026/06/24/apis-iq-medical-devices/ □Please also check related products and catalogs□

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Even in a rapidly changing world, the philosophy of HuLinks has not changed since its founding. The greatness of humanity lies in our ability to think, create, and carve out a new tomorrow. We aim to contribute to society by providing carefully selected solutions that support this remarkable human ability—intellectual creation—while also offering a more comfortable environment and enhancing productivity.

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