Focus group and survey confirm growing complexity of drug development and increasing adoption of smarter clinical trials Tom Parke, Head of Clinical Technologies, Tessella I was lucky enough to join a focus group at the recent 8th Annual SAS Health Care & Life Sciences Executive Conference (http://www.sas.com/news/preleases/hlsconf-clinicaltrials.html). The group comprising of selected pharmaceutical industry executives, [...]

Tessella is a gold sponsor of the 2012 Bio-IT World Conference taking place at the World Trade Centre in Boston on the 24th and 26th of April 2012. If you would like to have a prearranged meeting with Tessella at the event then please email info@tessella.com. To find out more about Bio-IT World Conference 2012, visit [...]

Your copy of tessella news Spring/Summer 2011 edition is available for download: http://www.tessella.com/wp-content/uploads/publications/tessellanews_issue72.pdf. In this edition: The National Archives and Tessella win Queen’s Award for Enterprise Unique public-private partnership recognised for innovation by UK’s most prestigious business awards. Read more (PDF). Unilever rationalise support and extend value of legacy scientific applications When Unilever needed to [...]

Wellcome Trust’s large-scale digitisation programme picks Tessella’s SDB to manage digital assets Oxford, UK | 10 May 2011. Tessella, the international provider of science powered technology and consulting services is pleased to announce that it has been selected by the Wellcome Trust to deliver a Digital Asset Management (DAM) using Tessella’s Safety Deposit Box (SDB), [...]

An Innovation award was made jointly to the official archive and technology provider, Tessella for their public private partnership in developing a system for preserving digital information. This system, the Safety Deposit Box (SDB), has since been adopted by libraries and archives around the world…read more

By Peter Mansell Growing implementation of adaptive clinical trials following the publication of draft guidance on adaptive designs by the US Food and Drug Administration in February 2010 is helping to ease regulatory concerns within industry about the approach, says eClinical solutions specialist Perceptive Informatics…read more