from feedback and good practices
quality methods and processes
more effectively with suppliers
the company around one of the quality approaches
the occurrence of nonconformities
quality activities and establish indicators
the management of quality actions
risks and opportunities
from feedback and good practices
quality methods and processes
more effectively with suppliers
the company around one of the quality approaches
the occurrence of nonconformities
quality activities and establish indicators
the management of quality actions
risks and opportunities
Anticipate, control and master your quality processes while ensuring quality expected by the market
Leverage documented information and manage its lifecycle
Prepare and control audits
Report deviations and ensure traceability
Integrate stakeholders in a quality approach
Establish a workflow to define problems and search for root causes
Define, manage and evaluate corrective and preventive actions (CAPA)
Anticipate, control and master your quality processes while ensuring quality expected by the market
Leverage documented information and manage its lifecycle
Prepare and control audits
Report deviations and ensure traceability
Integrate stakeholders in a quality approach
Establish a workflow to define problems and search for root causes
Define, manage and evaluate corrective and preventive actions (CAPA)
Quickly declare and ensure the traceability of nonconformities, customer complaints, and improvements
Associate events with a defects library and information from your product lifecycle management (PLM) or enterprise resource planning (ERP) system
Prioritize events by importance and urgency
Automate email notifications to the appropriate users
Report events wherever you are with the mobile application
Investigate with intuitive workflows such as the Eight Disciplines of Problem Solving (8D) or the Plan-Do-Check-Act (PDCA) cycle
Define problems according to the 5W1H questioning method (Who, What, When Where, Why, and How)
Search for root causes with an Ishikawa diagram
Implement immediate corrective and preventive actions for each root cause
Manage, monitor and evaluate actions from dashboards in a single reference system
Automatically generate reports
Quickly declare and ensure the traceability of nonconformities, customer complaints, and improvements
Associate events with a defects library and information from your product lifecycle management (PLM) or enterprise resource planning (ERP) system
Prioritize events by importance and urgency
Automate email notifications to the appropriate users
Report events wherever you are with the mobile application
Investigate with intuitive workflows such as the Eight Disciplines of Problem Solving (8D) or the Plan-Do-Check-Act (PDCA) cycle
Define problems according to the 5W1H questioning method (Who, What, When Where, Why, and How)
Search for root causes with an Ishikawa diagram
Implement immediate corrective and preventive actions for each root cause
Manage, monitor and evaluate actions from dashboards in a single reference system
Automatically generate reports
Gather all the documentation related to quality (ex. certificates, standards, procedures, reports, etc.) with electronic document management (EDM)
Version, archive, validate and distribute documents according to a configurable workflow with electronic signature
Search by keywords to document content, use advanced search tools, subscribe to content types, and manage access rights and mailing lists
Prepare audits based on themes and control points associated with procedures and compliance criteria
Plan resources and set deadlines
Structure internal audit forms
Automatically generate audit reports and trace discrepancies
Communicate with suppliers through a secure external portal
Automatically follow-up with suppliers on their eligible documents, action plans and responses to claims
Evaluate the performance of suppliers with configurable indicators
Gather all the documentation related to quality (ex. certificates, standards, procedures, reports, etc.) with electronic document management (EDM)
Version, archive, validate and distribute documents according to a configurable workflow with electronic signature
Search by keywords to document content, use advanced search tools, subscribe to content types, and manage access rights and mailing lists
Prepare audits based on themes and control points associated with procedures and compliance criteria
Plan resources and set deadlines
Structure internal audit forms
Automatically generate audit reports and trace discrepancies
Communicate with suppliers through a secure external portal
Automatically follow-up with suppliers on their eligible documents, action plans and responses to claims
Evaluate the performance of suppliers with configurable indicators
Capture, structure and ensure consistency of the design data throughout the design process
Manage the activity of the project team, and automatically generate summary and statistical documents
Leverage know-how through cumulative generic studies
Manage business risks and opportunities according to various quality assurance reference standards such as:
Manage action plans
Use graphical functional modeling tools such as Octopus, Cross Sorting, FAST, etc.
Structure and reuse functional specifications ensuring the traceability of modifications
Capture, structure and ensure consistency of the design data throughout the design process
Manage the activity of the project team, and automatically generate summary and statistical documents
Leverage know-how through cumulative generic studies
Manage business risks and opportunities according to various quality assurance reference standards such as:
Manage action plans
Use graphical functional modeling tools such as Octopus, Cross Sorting, FAST, etc.
Structure and reuse functional specifications ensuring the traceability of modifications
Ensure total quality by eliminating the root causes of nonconformities and anticipate risks
Reduce costs by optimizing and automating processes
Set the appropriate quality procedures to meet the requirements of standards and regulations
Build customer loyalty with satisfactory product quality and responsiveness to complaints
Whether in the automotive, aerospace, railway or naval sectors, quality in vehicle production involves many different scopes.
Our solution allows you to keep control of your quality process in sectors combining highly technical products, long life cycle and small series production.
Meet your safety requirements and limit the risks to production and passengers.
TEEXMA® for Quality supports electrical, nuclear and renewable energy industries in their quality control process.
Improve your overall performance and the safety of your infrastructures by responding efficiently to non-conformities.
Process all corrective and preventive actions according to configurable workflows, whatever their level of complexity and manage interventions even on extended networks via the mobile application.
TEEXMA® for Quality offers you a complete traceability of your equipment and incidents and a capitalization of the experience in order to optimize your quality process.
There are currently 1400 standards related to the healthcare field, and certification/accreditation, control or quality management issues are among the top.
We support you in your efforts to strengthen your quality and compliance processes, whether you are a pharmaceutical company with the ISO IDMP series, a medical device company with the ISO/TC210 standards or a health care center.
Whether in the automotive, aerospace, railway or naval sectors, quality in vehicle production involves many different scopes.
Our solution allows you to keep control of your quality process in sectors combining highly technical products, long life cycle and small series production.
Meet your safety requirements and limit the risks to production and passengers.
TEEXMA® for Quality supports electrical, nuclear and renewable energy industries in their quality control process.
Improve your overall performance and the safety of your infrastructures by responding efficiently to non-conformities.
Process all corrective and preventive actions according to configurable workflows, whatever their level of complexity and manage interventions even on extended networks via the mobile application.
TEEXMA® for Quality offers you a complete traceability of your equipment and incidents and a capitalization of the experience in order to optimize your quality process.
There are currently 1400 standards related to the healthcare field, and certification/accreditation, control or quality management issues are among the top.
We support you in your efforts to strengthen your quality and compliance processes, whether you are a pharmaceutical company with the ISO IDMP series, a medical device company with the ISO/TC210 standards or a health care center.
The concerns around a quality approach in an industrial company are diverse, ranging from improving customer satisfaction to optimizing the production process, or improving the overall quality of products.
Whether your objective is to be ISO 9001 certified or to improve the efficiency of your structure, TEEXMA® for Quality supports you in your quality management process.
Our solution is approved in many sectors, from mechanical components to chemicals, from raw materials to luxury goods.
The problem of the organization of a laboratory is essential. Centralize all quality procedures related to your laboratory in an internal and external document repository.
TEEXMA® for Quality is suitable for quality control and R&D laboratories by structuring your incidents and CAPA management.
Meet the requirements of the ISO 17025 standard by simply managing non-conformity events on materials or equipment, and by associating them with tests or samples.
The concerns around a quality approach in an industrial company are diverse, ranging from improving customer satisfaction to optimizing the production process, or improving the overall quality of products.
Whether your objective is to be ISO 9001 certified or to improve the efficiency of your structure, TEEXMA® for Quality supports you in your quality management process.
Our solution is approved in many sectors, from mechanical components to chemicals, from raw materials to luxury goods.
The problem of the organization of a laboratory is essential. Centralize all quality procedures related to your laboratory in an internal and external document repository.
TEEXMA® for Quality is suitable for quality control and R&D laboratories by structuring your incidents and CAPA management.
Meet the requirements of the ISO 17025 standard by simply managing non-conformity events on materials or equipment, and by associating them with tests or samples.
