If you work in a manufacturing facility, we’ve got a product offering that can change your life. Sounds like a lofty promise, doesn’t it? Our answer is all about one of the most unique of our offerings at Radwell International: our Radwell Verified Sub Program. It is not something that is all that common to find among industrial automation service/parts providers. We get asked about this program all the time by customers who want to know what a Radwell Verified Sub is and how it can benefit them.

Radwell Manufactured Verified Substitutes are high quality, brand new replacement industrial automation products that are the equivalent of the original manufacturer’s equipment. With savings of up to 85% on the original part, Radwell’s customers are benefiting from huge cost savings, a market leading 3-year warranty and 24-hour shipping on a range of extensive stock.

In this day and age, human machine interfaces (HMIs) are everywhere. Think about every point of contact a human has with technology and it becomes a reminder that as humans, we interact with machines in just about every aspect of our lives. Self-service checkouts at supermarkets, using a SAT NAV or getting some cash at cash machines are all examples of instances when humans interact with an interface designed to help foster human/machine communication.

Achieving an ISO Certification is a lengthy and detailed process. A positive result is very important for a company, as well as the customers it services.

The ISO 9001:2015 Certification is a globally recognised award that ensures customers have the confidence that organisations will meet their service requirements and deliver quality products. This achievement is very important for a company as well as the customers it serves.

There are many important things to consider when choosing an electronics repair company to work with. The right repair company for your business can ensure that your repair process is efficient and seamless. Keeping your business up and running can be a matter of choosing the right company to handle your repairs. 

When the European Union's (EU's) Medical Device Regulation (MDR) was first introduced in 2017, it set in motion a three-year countdown to its full application in 2020. The MDR could drastically impact the way medical devices are made in the EU, particularly those produced using additive manufacturing (AM).