Resource Centre: Latest Updates
The 5 types of 3D scanning technology
From scanning an object to reverse engineering it, there are many ways to use 3D scanning to benefit your manufacturing. Discover the 5 different types and advantages for each one in our whitepaper.
Read moreGetting drug-device combinations to market
The key to getting drug-device combinations to market compliantly is in the classification of the product. But what other considerations are applicable?
Read moreWhen, why, and how to best utilise 3D printing
With the ability to 3D print anything from a house to a bionic arm it’s difficult to know when, why and how to best utilise 3D printing. The question is: when you can make anything you need, what do you need to make?
Read moreFinding the right D&D partner
Design and development (D&D) of a medical device is the most crucial phase of the product’s route to market for its success. Why is it important to partner with an expert?
Read more7 benefits of working with UK medical device manufacturers
93% of consumers say they’re willing to pay extra for British-made products. From reducing your business’ emissions to experiencing shorter lead times, discover the pros to working with UK manufacturers.
Read moreKey considerations for medical device packaging
Medical device packaging is often overlooked by many businesses, but there are a lot of things to consider. From materials to sterilisation, discover the key factors to think about.
Read moreUsing ultrasonic welding as your manufacturing solution
A quick and efficient way to bond two thermoplastic components, ultrasonic welding is a popular solution in manufacturing medical devices. But why? We delve into the benefits…
Read moreHow to solve injection moulding problems
Get to the bottom of any issues with injection moulding processes efficiently and discover the right approach and problem-solving tools outlined in our whitepaper.
Read moreThe must-know clinical evaluation requirements
With the new European Union Medical Device Regulation (MDR 2017/745) replacing the Medical Device Directive (MDD 93/42/EEC) in May 2021, the requirements for clinical evaluation have changed. Read our whitepaper to understand how you’re affected.
Read more