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European Pharmaceutical Contractor

epc
Spring 2017

   
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Data Management & IT Solutions
Spotlight

Transforming Software


Bracket’s Steve Rawbone and Stephane Deleger highlight the advantages of iterative design and user acceptance testing, detailing how this can reduce the complexity of clinical trials.
 
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DATA MANAGEMENT
Electronic Data Interchange

Destination: Automation


A hands-off approach to trials, through to the automation of processes such as the managing of inventories, is a new industry goal, but Ian Davison at HMD Clinical suggests that this raises its own questions.
 
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Supply Chain Management
Supply Management
 
Getting Interactive


Utilisation of intelligent IRT systems is the best way to meet the demands of clinical supply management, argues Stefan Dürr at Cenduit, as this can save time and eliminate unnecessary work.
 
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Local Trial Supply

The Hungarian Way


Many countries in the CEE region are now looking to local companies for several supply activities, so Tibor Kovacs at PharmaRoad expands on the reasons why Hungary is leading this trend.
 
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Managing Risk

Risky Business


Nils Markmann at World Courier explains how manufacturers can prepare for growing challenges in the modern mobile supply chain, protecting both themselves and patients.
 
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Published quarterly in
February, May,
August and November

News and Press Releases

When space is tight

Existing packaging lines can be retrofitted for serialization tasks, achieving a maximum of space savings and process reliability: if required, the system comes with an integrated checkweigher and tamper-evident labeler.  
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White Papers

Running Better Trials Taking an Intelligent Monitoring Approach

Bioclinica

When it comes to implementing a risk-based monitoring program, it is not just about reducing monitoring visits and doing less Source Document Verification (SDV). It’s about bringing together your people, a solid process, and the right technology to run a better trial. Success with risk-based monitoring requires the ability to make sense of the thousands, if not millions, of data points captured by multiple disparate sources in a clinical trial. With the sheer volume of data generated on a daily basis comes complexity. How does one make sense of it all? Information overload burdens even the most experienced study teams who struggle to understand which data matters most and what it means.
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Industry Events

T3: Trials, Tech and Transformation

30-31 May 2018, Raleigh Convention Center, Raleigh, NC

T3 is back for 2018 to provide you with the latest updates and top tips from across the clinical trials landscape. Connecting leading experts, influencers and innovators from pharma, biotech, CROs, patient advocacy groups, academia and beyond, T3 is themeeting place for all stakeholders to voice their questions, connect with peers, and get direct feedback from an expert speaker line-up.And this year, we're in Raleigh.
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