Getting medical devices regulated to international standards is not easy. Rose explains how this process could be made much simpler.
Kiron explores why surgical practice needs to become more sustainable and considers some of the short and long-term actions that may make this a reality.
Graham looks at how companies can use this time of accelerated change to experiment with new, more effective ways of doing business.
The ISO 11608 series of standards are undergoing fundamental change – what should parenteral device companies be expecting?
A key factor in the sustainability of a product is its lifetime. How do we test a design to predict how long a new product will last?
CDP make a considerable investment in new facilities in North Carolina’s Research Triangle