An Overview of the Typical Information Required to Create a MIB
Introduction Why your device is needed/where your device is needed e.g. clinical setting Problems that your technology addresses/ Benefits that … read more »
Conformity Assessment
The assessment route you take depends on the classification of the device. You can determine your products’ class on the … read more »
CE Marking
The letters “CE” are the abbreviation of French phrase “Conformité Européene” meaning “European Conformity”. CE Marking is a symbol used on … read more »
The Drug Tariff – Creating a Successful Application
Reimbursement of medical devices for use in primary care in England and Wales is primarily based on Part IX of … read more »