We are now accepting tender applications for our planned laboratory expansion. More details can be found here.
The Medical Device Regulation 2017/745 (MDR) is replacing the current Medical Devices Directive 93/42/EEC (MDD) and the Active Implantable Medical Devices 93/42/EEC (AIMD). Read our post to find out how this affects you and how we can help
We are pleased to announce we are now UKAS accredited for EN 62368 and also EN 60601-1-11: 2015. Please click for more information on these standards and how we can help you.
The Government have recently published an update regarding the use of the CE mark and the new UKCA (UK Conformity Assessed) mark. Read our post for some important information.
We have updated our policy for customers who wish to visit us during the testing of their products. Please click the link to read a short update.
Read this short blog to have a look at what we can do for your company.
How do you prove your product meets Conformity Requirements? Have a look at our Technical File Review to make things clearer.
