

Upgrade
Upgrading a machine has no downsides. The level of automation increases, making your machine less prone to errors and process products fastly and reliably. GTE has a lot of experience in upgrading machines. Take Nelipak’s Blister seal machine, for example. We expanded this for a number of customers with an automatic sheet feeder as well as a printing station for printing the Tyvek lids. GTE’s expertise with printing Tyvek lids really helped these upgraded machines shine.

Why choose to upgrade and refurbish?
Upgrading an existing machine automates your production process (even) further. This makes the process more efficient and reduces the risk of errors. An additional advantage is that upgrading can also increase sustainability: as fewer mistakes occur, less material is wasted. Refurbishing machines has the advantage of longer-lasting machines, meaning you won’t have to buy a completely new one.
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Looking for something different? Take a look at GTE Custom-Made!
Are you looking for a specific machine that hasn’t been listed on our website? Take a look at GTE Custom-Made! GTE Custom-Made is a line of machines designed for specific purposes and fully customised to your needs.
Discover our knowledge & Inspiration

Whitepaper: Everything about vision systems in the pharmaceutical and medical industry
Precision and accuracy are extremely important. Whether they are used for correctly labeling products, or verifying the integrity of packaging, vision systems play a crucial role in any production process. What are their strengths and limitations, how do you prepare for their implementation, and what will the future look like in terms of, for example, AI? We are happy to help you get started; download the free whitepaper!

The Importance of IQ, PQ, and OQ in Machine Construction for the Pharmaceutical and Medical Industry
In the pharmaceutical and medical industries, developing machines that meet the highest quality and regulatory standards is essential. Therefore, the steps of IQ (Installation Qualification), PQ (Performance Qualification), and OQ (Operational Qualification) are followed during the construction of these machines. These qualification tests ensure that machines meet the required standards for installation, operation, and performance, and they are a critical part of the validation process.
At GTE Engineering, we use a traceability matrix and provide support with FAT (Factory Acceptance Test) and SAT (Site Acceptance Test) protocols to make the validation process structured and efficient. This approach guarantees that all requirements are documented and that the machines meet the highest standards in the pharmaceutical and medical industries.

The LAP-C with Mecademic robot
GTE designed and built the LAP-C. A circular platform for assembling and/or packaging medical products. When we design the LAP-C as an assembly machine, we often use a Mecademic robot.

High mix low volume manufacturing
In the pharmaceutical industry, there is a growing demand for high mix low volume manufacturing (HMLV). HMLV signifies that medications and medical devices are increasingly being personalized, tailored more specifically to the patient: a greater variety of medical products combined in smaller quantities.

3D printing in engineering– thinking out of the box
Years ago, in 2001, GTE engineering embraced 3D printing for the creation process of its exclusive machines. Until then it was science fiction. Today we can no longer live without it. How do we use 3D printing at GTE and what advantages does it have?

What is ‘Smart Customization’?
ETO, CTO and Smart Customization. Terms that are more often used in mechanical engineering. But what do these terms mean? Everyone working in mechanical engineering should know what development these words describe.
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