New Product Development Management
Suite that allows to automate the New Product Development Management and its changes, guaranteeing standardization in the processes and management shared with the suppliers.
Focusing on compliance with ISO / IEC 17000, ISO / TS 29001, among others, this Suite allows full control over the project schedule, automatically informing those responsible to carry out their activities on time, as well as All documents changed due to changes in a fast and comprehensive way.
SIQ New Product Development Management Suite is composed of the following modules:
New Product Development Management
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Approval Process Management
The Approval Process (APQP) combines all documents related to a product structure (BOM, in “quality vision”). It offers a requirement tree containing all items in this product structure, as well as the result of all its document workflows.
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Process Flow
The Process Flow gathers all stages of a given process through a clear symbology, with the aim of showing, in an uncomplicated way, all flow of information that aim to improve the understanding of the processes, as well as the creation of standard norms of work to Be followed. The Process Flow has a list of phases dependent on each other, and each phase has one or more related FMEA Standard. In addition, because the Process Flow is versionable, it is possible to insert attachments when there is a need to insert engineering revisions, changes in job descriptions, responsibilities and authorities, for example.
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Control Plan
The Control Plan gathers critical characteristics about a product or process, in order to provide means to detect possible flaws in the item under analysis. After approval of the Process FMEA Workflow, the Control Plan can be prepared manually or automatically generated by the system. The rejection of a Control Plan reopens the Process FMEA, causing the Control Plan to be reopened after the new approval of the Process FMEA.
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Default Risk
DFMEA implements FMEA in the project scope. It predicts potential failures in product creation and allows you to define actions for causes in order to reduce Severity, Occurrence, and Detection indicators.
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Risk Management
It performs the forecast of possible failures in a systematized way, allowing to define strategic preventive actions and improvements, in order to reduce and manage the risks of an operation.
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BOM – Bill of Material
The purpose of the BOM (Product Structure) module is to provide a detailed record with information on all components, raw materials and items used to obtain a product, identifying all the precedence and correct quantity relationships for each item required. This module can integrate with the customer’s ERP.
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Q.I (Quality Instructions)
Organizes the guidelines for the control of the records that make up the Quality Management System (QMS). It covers all the identification, collection, indexing, access, archives, storage, maintenance and disposal of technical and quality records.