Clinica's Guide to UK Medtech 2008
The Guide to UK Medtech 2008, to be distributed at the Medica 2008 event in Dusselfdorf, Germany, explores issues such as innovation, public-private partnership, the NIC-Darzi review, and also focuses on Wales and Northern Ireland.
Friday 31 October 2008

Rina Wolf: Personalised medicine, "the present as well as the future"
In the first of Clinica’s People Profiles, Girija Shettar speaks to reimbursement and regulatory affairs professional Rina Wolf about her work and why she joined the diagnostics industry.
Monday 6 October 2008

Smith & Nephew in China - getting ready for a big future
Smith & Nephew is convinced that a position in the Chinese market is essential. S&N spokesperson Liz Hewitt speaks to Girija Shettar about the company’s plans.
Monday 6 October 2008

Heavy workload awaits European Commission officials
The European Commission's medical device experts are facing a particularly packed agenda after their return from summer holidays.
Monday 22 September 2008

Commission proposals threaten to "slow innovation", says EDMA
Many of the proposals in the European Commission's consultation paper on the recast of the medical device directives would lead to a substantial increase in the cost of regulation, both to the device industry and to regulators. These costs would not be justified and would damage the ability of companies ñ particularly SMEs ñ to develop the new products that patients and society in general need, writes Amanda Maxwell.
Monday 22 September 2008

Proposals for EU regulatory change: a labyrinthine puzzle
Did the European Commission expect an easy ride from industry on its proposed device directive recast initiative? Probably not. But the statements that have flooded in and been made public show an industry in shock and preparing for battle. Amanda Maxwell comments.
Monday 22 September 2008

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