What do all the certification changes mean for a European-based machinery builder such as Sumitomo (SHI) Demag supplying moulding systems, periphery equipment and robotics to customers located in Great Britain or Ireland?
Medical device manufacturers selling in the UK have new responsibilities post-Brexit. Will you be registered and represented in time for the 2021 UK MHRA Registration deadlines?
MedTech Europe warns that until challenges are resolved, roadblocks will continue to limit the sector’s ability to seamlessly supply certified devices under the new rules.
Audrey Turley, senior biocompatibility expert at Nelson Labs, explains the value for medical device manufacturers to understand ISO 10993-23 and how to navigate the transition from in vivo irritation testing to in vitro testing.
Following the IGNITE Summit 2020, a new report sets out a series of “key game changers” to help build a resilient, prosperous and pioneering world-leading health innovation system.
