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article: Challenges and Trends in Clinical Research
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Industry Events

The European Medical Devices Regulation

27-28 January 2015, Metropole Hotel, Brussels, Belgium

Since the European Commission released a proposal for the new European medical device regulations in September 2012, industry has been attempting to gain a firm idea of what needs to be done to ensure preparation and compliance.
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News and Press Releases

New Approach to Delivering ‘Single Source of Truth’ Bridges Content Gaps across the Life Sciences Enterprise

BARCELONA, SPAIN – 18 Nov., 2014 – Veeva Systems introduces a breakthrough in regulated content management for life sciences with recent Veeva Vault innovations. Vault now delivers a single source of truth across the enterprise, uniting teams from research and development to commercial, to enable global harmonisation. Individuals throughout the organisation can share and reuse approved content, eliminating manual hand-offs and duplicate work. At the same time, Vault provides local autonomy and flexibility for each department or region to manage its own content to reflect its unique business processes. Vault maintains one authoritative source document in the cloud to bridge content gaps, increasing efficiency, visibility, and compliance.
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