
Scientists are developing highly innovative uses for both old and new materials in medical devices. Catherine Park investigates.

The issue of regulation is one that shadows the industry. For all of the concerns that it stifles innovation and threatens to drown the industry in bureaucracy it helps to set the standards, providing clear guidance on expectations.
Part of that process is the auditing of a manufacturing facility. What many people don't realise, according to Norm Howe of the VCI, is that the auditing starts as the inspectors enter the grounds, as he explains to Nic Paton.
Also in this issue, the MDMA's Thomas C Novelli delves into what is fast becoming the murky world of healthcare reform. The proposed device tax, new legislation and concerns over what constitutes effective research are raising concerns about a sustainable product pipeline.
In our cover story Professor Kevin Shakesheff explains the growing interest in regenerative medicine. It seems almost a million miles away from traditional manufacturers but the paths of these two innovative sectors are sure to cross.