The US Food and Drug Administration has provided $2.8m in funding for the...
ISO 10993-10: The Role of IATA Approach in Sensitization Assessment
This February ISO/TC 194 published the long-anticipated draft of ISO 10993-10
standard, named: “Biological evaluation of medical devices – Part 10: Tests for skin
The Importance of Accurately Measuring the Moisture Content of Plastic Resin in the Molding Process of Medical Devices
Moisture content is an important variable that must be monitored for and controlled during the production of plastic medical device parts.
Adder Launches New Range of NIAP PP 4.0 Secure KVM Switches and Accessories
Adder Technology, a global leader in connectivity solutions and high-performance IP KVM, has today announced the launch of the new ADDERView™ Secure Range of KVM switches and accessories.
Matrix – High Performance IP KVM
KVM (keyboard, video, mouse) switch technology was first introduced to the market in the 1990s as a method of controlling multiple computers with a single keyboard, video and mouse.
Adder Delivers Real-Time Control of Physical and Virtual Machines
Adder Technology, a global leader in connectivity solutions and high-performance IP KVM, announced the latest addition to its highly successful ADDERLink INFINITY range, the ADDERLink INFINITY 3000 (ALIF3000).
Back to compliance: MDIC extends a helping hand to struggling manufacturers
The US Food and Drug Administration has provided $2.8m in funding for the Medical Device Innovation Consortium to expand its Case for Quality Voluntary Improvement Program to device manufacturers with a history of quality violations. But, how will the process work, and how could the extra scrutiny bring non-compliant facilities back into the FDA’s good graces?
Driving towards the implementation of the new Medical Devices Regulations (MDR)
On 5 April 2017, two new Medical Devices Regulations (MDR) on medical devices were adopted, and they entered into force on 25 May 2017.
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