#digital work instructions

Ansomat: the company that thinks with you

Smarter production starts here

What if your shop floor no longer tolerates mistakes? If every screw is in the right place, every action is properly logged, and even a new operator immediately knows what to do? That’s not a dream for the future — it’s what Ansomat makes possible today.

Ansomat is a Belgian technology company with deep practical experience. Since 1996, they’ve been building digital solutions for the manufacturing industry. Not distant software, but tools that precisely meet what production companies really need: clarity, speed, and above all, reliability.

Ansomatic: your digital work partner

At the heart of their offering is Ansomatic, a platform that feels like a smart work partner. No more worn-out manuals or outdated process binders, but clear, visual instructions on a screen. Your operator doesn’t need to search or guess — Ansomatic shows exactly what needs to be done, step by step. Every detail is correct.

What makes it even better? Ansomatic works in sync with your machines. It reads sensors, checks via cameras whether a part is correctly placed, and only allows the process to continue when everything is right. No extra inspections, no time lost. Everything flows with maximum certainty.

People remain central

You might think: with all this technology, won’t people become less relevant? Not at Ansomat. On the contrary. Their system is designed to empower people, not replace them. Thanks to Operator Guidance, even new employees can get to work immediately. They receive clear instructions and make fewer mistakes. This means less pressure, more confidence, and faster independence.

Through Human Analytics, you also gain insight into where processes run smoothly, where delays occur, and where extra support is needed. This isn’t about control for the sake of control, but insights that help you train better, improve more effectively, or even rethink how work is organized.

For every screw, in every sector

Ansomatic is already in use across diverse production environments: from aerospace to automotive, from heavy machinery to electronics. In each of these sectors, reliability is key. One mistake can cost thousands of euros or compromise safety.

That’s why the system works just as well in a small work cell as it does in a fully automated production line. It’s flexible, scalable, and always focused on your specific needs.

Thinking alongside the best

Ansomat doesn’t build in isolation. They work with international technology partners such as Cognex and customers like Spirit AeroSystems. Together, they continuously improve the platform. Their approach has proven successful, as shown by international recognition: the company won the BLCC Golden Bridge Award as "Best Tech Company."

The next Step? Just take it

Want to make your production process smarter, safer, and more consistent? Now is the time. Request a demo and discover how Ansomatic seamlessly adapts to your company, your people, and your way of working.

Smarter production doesn’t start by changing everything. It starts by changing what matters. And Ansomat helps you do that, step by step, just like their platform.

Standard Work Pro is built for factories that want to move beyond outdated SOPs and inconsistent training.

It helps when your operators are doing the same task in five different ways, new hires struggle to follow printed instructions, or changes never make it to the floor in time.

Quality management systems are processes which help businesses comply to certain requirements and cut expenses. It was not easy in the past to implement the quality management system in an ERP. If the business has the required requirements, it's feasible to incorporate a QMS within the ERP software. The good news is that the QMS is generally low-cost and easy to use.

It is crucial to choose the appropriate size QMS that is appropriate for your organization. It's crucial to pick the right size QMS for your company. For this to be achieved the best approach is to adopt a gradual approach to documentation and build it out in time. If you don't have a strategy for documenting, it could result in inadequate documentation and can become burdensome. An effective quality management process that is phased can benefit your business.

It's important to define your system's requirements and then document its components. Include protocols, full specifications and acceptance requirements. It must be tested to ensure that it is compliant with the standards. Every test result should be recorded and reviewed by the person using the system. Furthermore every reviews and validations must be carried out quality management system by responsible personnel. Final, all conclusions must be made based upon findings and acceptance criteria. It is essential to avoid gaps in the system, or grey areas.

ISO/IEC 20000 has been a recognized industry-wide standard that is based on the QMS approach. The standard defines formal systems for control as well as traceability. It also stresses the significance of control procedures. GAMP Guide Another industry standard, explains the needs and capabilities of software manufacturing. The guide also outlines a management commitment to quality and control of design. The GAMP Guide also outlines the roles played by users as well as suppliers. It also outlines the roles of suppliers and users. GAMP Guide also lists test locations.

The digital quality control is the primary step of achieving Quality 4.0. This includes AI, machine-learning, big data and real-time production data. It improves transparency across all levels of the organization and tracking. Digital quality assurance aims to provide seamless experience for users. Quality assurance through digital technology not only decreases the number of defects, but also boosts efficiency, OEE, and compliance. It is an essential part of quality control in smart-connected factories.

Documentation is another important aspect of quality management methods. Documentation is a crucial component of a quality management system. It should be accessible and searchable in accordance with ISO 9001:2015. Documents need to be organized in a way they demonstrate that the quality process was followed correctly and that the results were in line with the quality standards. In addition, they must be kept up-to-date and available to anyone in the company. They may pose a risk for the whole system if they're not properly maintained. The entire QMS may fail if documents are not up to the standards.

In addition to documentation, cycle documentation best practices can be beneficial for various categories of systems. They are helpful for retrovalidating legacy systems as well as demonstrating conformance with GxP. Documentation of the cycle is essential for maintaining and developing software. The documents that pertain to quality assurance and documenting must be maintained within a quality assurance documentation management system. Documents should be available to be inspected. The quality system will be utilized in order to enhance the effectiveness of the company as well as sustainability.

Documenting processes and procedures for an effective quality management system (QMS) is an essential component to any QMS. Documentation must be provided of any kind and may include specifications to cover multiple processes. Quality management software can be used to document the procedure. The documentation should be precise and complete, and contain sufficient evidence to demonstrate objectively the quality management program is functioning. This article will outline a number of key documents that are crucial components of a QMS.

The quality management system outlines the process, stakeholder infrastructure, stakeholder, and process required to reach the goal. It provides a detailed picture of the organization's arrangement. This information is outlined Great post to read using a flow chart diagram, or other similar tools. The QMS recognizes those processes that require equipment, like employees or machines as well as technology. They are also recognized by the QMS. The QMS is able to be modified based on the size of an organization. is.

It is the ISO 9000 family covers various aspects of quality control. ISO 9001 is one of the most well-known standards. It lays out the essentials for quality control systems and is easily implemented by all companies. The certification was granted to more than 1 million companies and more than 170 nations. An organization can reap many benefits from this certification. It also demonstrates an organisation's effectiveness in meeting their obligations, ISO 9001 also promotes customer satisfaction.

QMS enhances satisfaction of customers while eliminating guesswork. It's possible to measure customer satisfaction, record the process and identify the areas in need of improvement. A company that consistently delivers quality will retain customers and enhance its image. QMS simplifies the administration of training records and analyzes resource requirements to speed up the process of onboarding. QMS also reduces customer complaints and improves customer satisfaction.

Quality management systems can increase efficiency and guarantee compliance with the regulations. They can also assist in developing an atmosphere that is driven by quality. A quality management system is crucial for all life science businesses. It must determine and set quality targets be in compliance with the laws and identify possibilities to enhance. This must be accomplished by the QMS. For example, it must include a well-defined implementation plan, and an annual quality review.

The QMS manual should contain general information as well as a comprehensive description of the system. The documents should also outline the nature of the QMS and include documented procedures, guidelines, and interactions between them. The quality manual is like the card you use to promote your quality management system. It should also be an informational library for marketing. It should be simple to understand and read. It should also include organizational diagrams and other graphs. If you plan to utilize the QMS It is essential to adhere to the ISO guidelines.

An extensive strategy for managing change is vital to ensure an up-to-date QMS. The plan outlines the reason of the process, actions, and activities necessary to carry out the change. The plan also outlines the timeframe as well as who's responsible for updating it. Quality plans are typically used to implement any changes to QMS. There's a process called change management which helps make this procedure smooth. This ensures all documentation and products are up-to-date.

A third and crucial aspect of the quality management system is organization. The structure of the organization should be documented , and it should cover all stages of the product development process, as well as concerns about quality that might occur. The documentation of processes should contain the flowcharts that show workflow as well as clearly delineated roles. It should also be accompanied by operational guidelines. Data management that is of high quality is essential to the overall QMS framework. A absence of proper data management could result in inconsistent quality of the product as well as compliance risk and reduced profits.

Implementing the QM program should not take more than one year. The process should be approached with clear goals, defined sources and strategies to achieve these goals. Managers should be in charge of the entire project to ensure they achieve their goals within the timeframe and that they have sufficient resources. A QM method cannot be considered a singular project. It should be a part of the overall strategy and culture.